Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rajasekaran Parthasarathy"'
Autor:
Rajasekaran Parthasarathy, Samson Jegan Jenniefer, Packianathan Thomas Muthiah, Nagarajan Sulochana
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 2, Pp o536-o536 (2012)
In the title crystal structure, C10H16O2, inversion-related molecules are linked by pairs of O—H...O hydrogen bonds involving carboxyl groups to form R22(8) dimers. The cyclohexene ring displays a half-chair conformation.
Externí odkaz:
https://doaj.org/article/21e26c02002140539affbc9d532cb5e4
Autor:
Nagarajan Sulochana, Packianathan Thomas Muthiah, Samson Jegan Jenniefer, Rajasekaran Parthasarathy
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 10, Pp o2732-o2732 (2011)
In the crystal of the title compound C10H17NO, synthesized by the reaction of β-cyclocitral with hydroxylamine hydrochloride, inversion-related molecules are linked by a pair of O—H...N hydrogen-bonding interactions between the oxime functionaliti
Externí odkaz:
https://doaj.org/article/8750d5560e2844dfb997d2204daf3c7d
Autor:
Rajasekaran, Parthasarathy, Samson Jegan, Jenniefer, Packianathan, Thomas Muthiah, Nagarajan, Sulochana
Publikováno v:
Acta Crystallographica Section E: Structure Reports
In the title crystal structure, C(10)H(16)O(2), inversion-related mol-ecules are linked by pairs of O-H⋯O hydrogen bonds involving carboxyl groups to form R(2) (2)(8) dimers. The cyclo-hexene ring displays a half-chair conformation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac0c76411f575c0ddbe1034d12983324
https://pubmed.ncbi.nlm.nih.gov/22347132
https://pubmed.ncbi.nlm.nih.gov/22347132
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 10, Pp o2732-o2732 (2011)
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E: Structure Reports
In the crystal of the title compound C10H17NO, synthesized by the reaction of β-cyclocitral with hydroxylamine hydrochloride, inversion-related molecules are linked by a pair of O—H...N hydrogen-bonding interactions between the oxime functionaliti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b0611cdc77b40193f5a125b610cdeee
http://scripts.iucr.org/cgi-bin/paper?S1600536811037895
http://scripts.iucr.org/cgi-bin/paper?S1600536811037895
Publikováno v:
Flavour & Fragrance Journal. Mar2016, Vol. 31 Issue 2, p120-123. 4p.