All bond lengths and anlges in the title compound, C 15 H 9 F 5 N 2 O 2 , an inhibitor of chitin synthesis, are normal. The urea linkage adopts an essentially planar con®guration, with an intramolecular NÐHÁ Á ÁO hydrogen bond. Intermolecular NÐHÁ Á ÁO hydrogen bonds link two adjacent molecules into
Ethyl 3-methyl-6-oxo-5-[3-(trifluoromethyl)phenyl]-1,6-dihydro-1-pyridazineacetate
✍ Scribed by Xu, Han ;Song, Hai-Bin ;Yao, Chang-Sheng ;Zhu, You-Quan ;Hu, Fang-Zhong ;Zou, Xiao-Mao ;Yang, Hua-Zheng
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 219 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
The title compound, C 25 H 26 O 2 , was isolated and characterized as a stable intermediate in the conversion of 2,2-diphenylethyl 2,4,6-trimethylphenyl ketone to its formaldehyde-derived enone.
In the title compound, C 28 H 27 N 3 O 3 , the pyrazolone ring and the N atom of the 2-amino-3-phenylpropanoate group are essentially coplanar. The compound is in an enamine-keto form and its structure is stabilized by one strong intramolecular N-HÁ Á ÁO hydrogen bond.
In the title compound, C 18 H 21 NO 4 , the molecules form dimers by means of a pair of NÐHÁ Á ÁO hydrogen bonds. The 2(1H)pyridone ring displays a screw±boat conformation.