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What would the chemical name be for C13H8Cl3NO

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What would the chemical name be for C13H8Cl3NO


How would you name this organic compound?What is the rationale of the IUPAC name for DDT?What would the name and formula be for Mo+O+Se?Chemical name : MelamineWhat would the name of this organic compound be?What is the chemical name of the compound H2S4O?What is the iupac name for ch3ch2cooag?What is the chemical name of this derivative of aniline?IUPAC Name for the following?What would be the name of this compound?













2












$begingroup$


enter image description hereFormula




C13H8Cl3NO




SMILES




C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl




I found the diagram on the left in a book and drew the one on the right using



https://pubchem.ncbi.nlm.nih.gov/edit2/index.html



And got the SMILES description from that.



Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.



Is there a automatic naming engine out there?



A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137






organic-chemistry nomenclature molecular-structure







share|improve this question











$endgroup$








  • 1




    $begingroup$
    Try Chemspider chemspider.com
    $endgroup$
    – Waylander
    2 hours ago






  • 1




    $begingroup$
    Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
    $endgroup$
    – matt_black
    2 hours ago






  • 2




    $begingroup$
    @matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
    $endgroup$
    – Mithoron
    2 hours ago






  • 3




    $begingroup$
    @matt_black That's Chemdoodle being Chemdoodle, I think:)
    $endgroup$
    – andselisk
    2 hours ago
















2












$begingroup$


enter image description hereFormula




C13H8Cl3NO




SMILES




C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl




I found the diagram on the left in a book and drew the one on the right using



https://pubchem.ncbi.nlm.nih.gov/edit2/index.html



And got the SMILES description from that.



Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.



Is there a automatic naming engine out there?



A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137






organic-chemistry nomenclature molecular-structure







share|improve this question











$endgroup$








  • 1




    $begingroup$
    Try Chemspider chemspider.com
    $endgroup$
    – Waylander
    2 hours ago






  • 1




    $begingroup$
    Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
    $endgroup$
    – matt_black
    2 hours ago






  • 2




    $begingroup$
    @matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
    $endgroup$
    – Mithoron
    2 hours ago






  • 3




    $begingroup$
    @matt_black That's Chemdoodle being Chemdoodle, I think:)
    $endgroup$
    – andselisk
    2 hours ago














2












2








2





$begingroup$


enter image description hereFormula




C13H8Cl3NO




SMILES




C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl




I found the diagram on the left in a book and drew the one on the right using



https://pubchem.ncbi.nlm.nih.gov/edit2/index.html



And got the SMILES description from that.



Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.



Is there a automatic naming engine out there?



A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137






organic-chemistry nomenclature molecular-structure







share|improve this question











$endgroup$




enter image description hereFormula




C13H8Cl3NO




SMILES




C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl




I found the diagram on the left in a book and drew the one on the right using



https://pubchem.ncbi.nlm.nih.gov/edit2/index.html



And got the SMILES description from that.



Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.



Is there a automatic naming engine out there?



A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137






organic-chemistry nomenclature molecular-structure




organic-chemistry nomenclature molecular-structure






share|improve this question















share|improve this question













share|improve this question




share|improve this question








edited 2 hours ago









andselisk

17k655115




17k655115










asked 2 hours ago









KalleMPKalleMP

389116




389116








  • 1




    $begingroup$
    Try Chemspider chemspider.com
    $endgroup$
    – Waylander
    2 hours ago






  • 1




    $begingroup$
    Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
    $endgroup$
    – matt_black
    2 hours ago






  • 2




    $begingroup$
    @matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
    $endgroup$
    – Mithoron
    2 hours ago






  • 3




    $begingroup$
    @matt_black That's Chemdoodle being Chemdoodle, I think:)
    $endgroup$
    – andselisk
    2 hours ago














  • 1




    $begingroup$
    Try Chemspider chemspider.com
    $endgroup$
    – Waylander
    2 hours ago






  • 1




    $begingroup$
    Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
    $endgroup$
    – matt_black
    2 hours ago






  • 2




    $begingroup$
    @matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
    $endgroup$
    – Mithoron
    2 hours ago






  • 3




    $begingroup$
    @matt_black That's Chemdoodle being Chemdoodle, I think:)
    $endgroup$
    – andselisk
    2 hours ago








1




1




$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago




$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago




1




1




$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago




$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago




2




2




$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
2 hours ago




$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
2 hours ago




3




3




$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
2 hours ago




$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
2 hours ago










2 Answers
2






active

oldest

votes


















5












$begingroup$

Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.



Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide






share|improve this answer











$endgroup$





















    2












    $begingroup$

    There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
    They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:




    enter image description here




    Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.



    References




    1. Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.






    share|improve this answer









    $endgroup$













      Your Answer





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      2 Answers
      2






      active

      oldest

      votes








      2 Answers
      2






      active

      oldest

      votes









      active

      oldest

      votes






      active

      oldest

      votes









      5












      $begingroup$

      Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.



      Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide






      share|improve this answer











      $endgroup$


















        5












        $begingroup$

        Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.



        Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide






        share|improve this answer











        $endgroup$
















          5












          5








          5





          $begingroup$

          Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.



          Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide






          share|improve this answer











          $endgroup$



          Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.



          Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide







          share|improve this answer














          share|improve this answer



          share|improve this answer








          edited 2 hours ago









          Loong♦

          33.3k883172




          33.3k883172










          answered 2 hours ago









          JustanotherchemistJustanotherchemist

          1,894620




          1,894620























              2












              $begingroup$

              There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
              They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:




              enter image description here




              Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.



              References




              1. Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.






              share|improve this answer









              $endgroup$


















                2












                $begingroup$

                There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
                They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:




                enter image description here




                Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.



                References




                1. Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.






                share|improve this answer









                $endgroup$
















                  2












                  2








                  2





                  $begingroup$

                  There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
                  They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:




                  enter image description here




                  Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.



                  References




                  1. Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.






                  share|improve this answer









                  $endgroup$



                  There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
                  They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:




                  enter image description here




                  Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.



                  References




                  1. Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.







                  share|improve this answer












                  share|improve this answer



                  share|improve this answer










                  answered 2 hours ago









                  andseliskandselisk

                  17k655115




                  17k655115






























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