๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Source of pyrrole-2-carboxylate in mammalian urine

โœ Scribed by Anne M. Heacock; Elijah Adams


Book ID
118854061
Publisher
Elsevier Science
Year
1973
Tongue
English
Weight
316 KB
Volume
50
Category
Article
ISSN
0006-291X

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


2-Hydroxycyclohexyl 1H-pyrrole-2-carboxy
โœ Dong, Li ;Yin, Zhen-Ming ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 291 KB
4-Pyridylmethyl 1H-pyrrole-2-carboxylate
โœ Wang, Wu-Yan ;Yin, Zhen-Ming ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 215 KB

The title compound, C 11 H 10 N 2 O 2 , has been synthesized by the reaction of 2-(trichloroacetyl)pyrrole with 4-(hydroxymethyl)pyridine. In the solid state, the molecules form a onedimensional infinite ladder structure through intermolecular N-Hร ร รN and C-Hร ร รO hydrogen bonds.

Ethyl 5-cyano-1H-pyrrole-2-carboxylยญate
โœ Zhang, Yan-Hua ;Yin, Zhenming ;Li, Xiao-Fang ;He, Jiaqi ;Cheng, Jin-Pei ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 156 KB

Single-crystal X-ray study T = 293 K Mean '(CยฑC) = 0.004 A รŠ R factor = 0.053 wR factor = 0.159 Data-to-parameter ratio = 12.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

Degradation of thiophene-2-carboxylate,
โœ Janet S. Evans; W. A. Venables ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer ๐ŸŒ English โš– 580 KB

A bacterium of the genus Vibrio, capable of degrading thiophene derivatives, was isolated from enrichment cultures inoculated with oil-contaminated estuarine mud. Of the thiophene derivatives tested, only thiophene-2-carboxylate (T2C), thiophene-2-acetate and thiophene-2-carbonyl chloride supported

Methyl 4-p-tolyl-1H-pyrrole-2-carboxylยญa
โœ Gardiner, Michael G. ;Jones, Roderick C. ;Ng, Sarah ;Smith, Jason A. ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 151 KB

The molecules of the title compound, C 13 H 13 NO 2 , are close to planar [maximum deviation of 0.0753 (15) A หšfrom the leastsquares plane defined by all non-H atoms in the molecule]. Molecules form centrosymmetric dimers through N-Hร ร รO hydrogen bonding. Molecules further associate through edgeto