Cargando…

6-Methyl­pyridin-2-amine

In the title mol­ecule, C(6)H(8)N(2), the endocyclic angles are in the range 118.43 (9)–122.65 (10)°. The mol­ecular skeleton is planar (r.m.s. deviation = 0.007 Å). One of the two amino H atoms is involved in an N—H⋯N hydrogen bond, forming an inversion dimer, while the other amino H atom participa...

Descripción completa

Detalles Bibliográficos
Autores principales: Draguta, Sergiu, Khrustalev, Victor N., Sandhu, Bhupinder, Antipin, Mikhail Yu., Timofeeva, Tatiana V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589040/
https://www.ncbi.nlm.nih.gov/pubmed/23476276
http://dx.doi.org/10.1107/S1600536812047800
_version_ 1782261683786350592
author Draguta, Sergiu
Khrustalev, Victor N.
Sandhu, Bhupinder
Antipin, Mikhail Yu.
Timofeeva, Tatiana V.
author_facet Draguta, Sergiu
Khrustalev, Victor N.
Sandhu, Bhupinder
Antipin, Mikhail Yu.
Timofeeva, Tatiana V.
author_sort Draguta, Sergiu
collection PubMed
description In the title mol­ecule, C(6)H(8)N(2), the endocyclic angles are in the range 118.43 (9)–122.65 (10)°. The mol­ecular skeleton is planar (r.m.s. deviation = 0.007 Å). One of the two amino H atoms is involved in an N—H⋯N hydrogen bond, forming an inversion dimer, while the other amino H atom participates in N—H⋯π inter­actions between the dimers, forming layers parallel to (100).
format Online
Article
Text
id pubmed-3589040
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-35890402013-03-08 6-Methyl­pyridin-2-amine Draguta, Sergiu Khrustalev, Victor N. Sandhu, Bhupinder Antipin, Mikhail Yu. Timofeeva, Tatiana V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(6)H(8)N(2), the endocyclic angles are in the range 118.43 (9)–122.65 (10)°. The mol­ecular skeleton is planar (r.m.s. deviation = 0.007 Å). One of the two amino H atoms is involved in an N—H⋯N hydrogen bond, forming an inversion dimer, while the other amino H atom participates in N—H⋯π inter­actions between the dimers, forming layers parallel to (100). International Union of Crystallography 2012-11-28 /pmc/articles/PMC3589040/ /pubmed/23476276 http://dx.doi.org/10.1107/S1600536812047800 Text en © Draguta et al. 2012 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
Draguta, Sergiu
Khrustalev, Victor N.
Sandhu, Bhupinder
Antipin, Mikhail Yu.
Timofeeva, Tatiana V.
6-Methyl­pyridin-2-amine
title 6-Methyl­pyridin-2-amine
title_full 6-Methyl­pyridin-2-amine
title_fullStr 6-Methyl­pyridin-2-amine
title_full_unstemmed 6-Methyl­pyridin-2-amine
title_short 6-Methyl­pyridin-2-amine
title_sort 6-methyl­pyridin-2-amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589040/
https://www.ncbi.nlm.nih.gov/pubmed/23476276
http://dx.doi.org/10.1107/S1600536812047800
work_keys_str_mv AT dragutasergiu 6methylpyridin2amine
AT khrustalevvictorn 6methylpyridin2amine
AT sandhubhupinder 6methylpyridin2amine
AT antipinmikhailyu 6methylpyridin2amine
AT timofeevatatianav 6methylpyridin2amine