The title compound, C~19~H~21~FN~3~O~3~PS, was synthesized by the reaction of __N__-benzylidene-5-(4-fluorophenyl)-1,3,4-thiadiazol-2-amine and diethyl phosphite. Intermolecular N—H...O hydrogen bonds connect molecules into centrosymmetric dimers.
(R)-Diethyl [(4-chlorophenyl)(5-m-tolyl-1,3,4-thiadiazol-2-ylamino)methyl]phosphonate
✍ Scribed by Wan, Rong ;Han, Feng ;Cao, Lin ;Zhang, Jin-Jun ;Wang, Jin-Tang
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 117 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
In the title compound, C 18 H 14 ClN 3 O 2 S 2 , the thiazolidine ring adopts an envelope conformation. There are intermolecular C-HÁ Á ÁO interactions, forming centrosymmetric dimers.
In the title compound, C 19 H 22 ClN 4 O 5 PS, the P atom adopts a distorted tetrahedral configuration. Intra-and intermolecular C-HÁ Á ÁO hydrogen bonds, together with weak C-HÁ Á Á hydrogen bonding and strongstacking interactions, stabilize the crystal structure.
In the title compound, C 21 H 24 ClN 4 O 5 P, the P atom adopts a distorted tetrahedral configuration. In the crystal structure, inter-and intramolecular C-HÁ Á ÁO hydrogen bonds contribute to the stability of the structure, andstacking interactions are also observed.
The title compound, C 18 H 12 F 3 N 3 OS 2 , was synthesized by the reaction of [(Z)-1-phenylmethylidene]{5-[3-(trifluoromethyl)phenyl]-1,3,4-thiadiazol-2-yl}amine and mercaptoacetic acid. In the structure there are intramolecular C-HÁ Á ÁS and C-HÁ Á ÁN and intermolecular C-HÁ Á ÁN hydrogen bonds.