Cargando…

(4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine

In the mol­ecule of the title homoallylic amine, C(16)H(13)ClF(3)N, the dihedral angle between the two benzene rings is 84.63 (4)°. Weak intra­molecular N—H⋯F hydrogen bonds generate S(6) and S(5) ring motifs. In the crystal structure, weak inter­molecuar N—H⋯F hydrogen bonds link mol­ecules into ce...

Descripción completa

Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Rai, Sankappa, Shetty, Prakash, Isloor, Arun M., Chantrapromma, Suchada
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977711/
https://www.ncbi.nlm.nih.gov/pubmed/21583847
http://dx.doi.org/10.1107/S1600536809012896
_version_ 1782191170022014976
author Fun, Hoong-Kun
Rai, Sankappa
Shetty, Prakash
Isloor, Arun M.
Chantrapromma, Suchada
author_facet Fun, Hoong-Kun
Rai, Sankappa
Shetty, Prakash
Isloor, Arun M.
Chantrapromma, Suchada
author_sort Fun, Hoong-Kun
collection PubMed
description In the mol­ecule of the title homoallylic amine, C(16)H(13)ClF(3)N, the dihedral angle between the two benzene rings is 84.63 (4)°. Weak intra­molecular N—H⋯F hydrogen bonds generate S(6) and S(5) ring motifs. In the crystal structure, weak inter­molecuar N—H⋯F hydrogen bonds link mol­ecules into centrosymmetric dimers which are arranged in mol­ecular sheets parallel to the ac plane.
format Text
id pubmed-2977711
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29777112010-12-30 (4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine Fun, Hoong-Kun Rai, Sankappa Shetty, Prakash Isloor, Arun M. Chantrapromma, Suchada Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecule of the title homoallylic amine, C(16)H(13)ClF(3)N, the dihedral angle between the two benzene rings is 84.63 (4)°. Weak intra­molecular N—H⋯F hydrogen bonds generate S(6) and S(5) ring motifs. In the crystal structure, weak inter­molecuar N—H⋯F hydrogen bonds link mol­ecules into centrosymmetric dimers which are arranged in mol­ecular sheets parallel to the ac plane. International Union of Crystallography 2009-04-10 /pmc/articles/PMC2977711/ /pubmed/21583847 http://dx.doi.org/10.1107/S1600536809012896 Text en © Fun et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Fun, Hoong-Kun
Rai, Sankappa
Shetty, Prakash
Isloor, Arun M.
Chantrapromma, Suchada
(4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
title (4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
title_full (4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
title_fullStr (4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
title_full_unstemmed (4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
title_short (4-Chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
title_sort (4-chloro-2-fluoro­phen­yl)[1-(2,6-difluoro­phen­yl)but-3-en­yl]amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977711/
https://www.ncbi.nlm.nih.gov/pubmed/21583847
http://dx.doi.org/10.1107/S1600536809012896
work_keys_str_mv AT funhoongkun 4chloro2fluorophenyl126difluorophenylbut3enylamine
AT raisankappa 4chloro2fluorophenyl126difluorophenylbut3enylamine
AT shettyprakash 4chloro2fluorophenyl126difluorophenylbut3enylamine
AT isloorarunm 4chloro2fluorophenyl126difluorophenylbut3enylamine
AT chantraprommasuchada 4chloro2fluorophenyl126difluorophenylbut3enylamine