CAS:2349-67-9|5-Amino-1,3,4-thiadiazole-2-thiol

Catalogue Number:A633300
Chemical Name:5-Amino-1,3,4-thiadiazole-2-thiol
Synonyms:2-Amino-1,3,4-thiadiazol-5-thiol; 2-Amino-1,3,4-thiadiazole-5-mercaptan; 2-Amino-1,3,4-thiadiazole-5-thiol; 2-Amino-5-mercapto-1,3,4-thiadiazole; 2-Amino-5-mercapto-1,3,5-thiadiazole; 2-Amino-5-mercaptothiadiazole; 2-Amino-Δ2-1,3,4-thiadiazoline-5-thione; 2-Mercapto-5-amino-1,3,4-thiadiazole; 2-Thiol-5-amino-1,3,4-thiadiazole; 5-Amino-1,3,4-thiadiazole-2(3H)-thione; 5-Amino-1,3,4-thiadiazole-2-thiol; 5-Amino-1,3,4-thiadiazole-2-thione; 5-Amino-1,3,4-thiadiazoline-2-thione; 5-Amino-1,3,4-thidiazole-2-thiol; 5-Amino-2-mercapto-1,3,4-thiadiazole; 5-Amino-3H-1,3,4-thiadiazole-2-thione; 5-Thio-2-amino-[1,3,4]thiadiazole; 5-Thiol-2-amino-1,3,4-thiadiazole; ATT; NSC 209061; NSC 21402; WR 180; Acetazolamide EP Impurity G
Impurity:Acetazolamide EP Impurity G
CAS Number:2349-67-9
Molecular Formula:C₂H₃N₃S₂
Appearance:White to Light Beige Solid
Melting Point:>227°C (Subl.)
Molecular Weight:133.19
Storage:20°C
Solubility:DMSO (Slightly), Methanol (Slightly)
Category:Building Blocks; Miscellaneous;
Applications:5-Amino-1,3,4-thiadiazole-2-thiol is a thiadiazole derivative with antibacterial acitivity used in the preparation of herbicides as well as carbonic anhydrase inhibitors. (Acetazolamide EP Impurity G)
References:Li, Z. et al.: Ying. Huax., 5, 54 (1988); Supuran, C. et al.: Rev. Roum. Chim., 40, 1227 (1995);
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