5-Amino-1,3,4-thiadiazole-2-thiol

CAS: 2349-67-9

Ref. TR-A633300

Product Information

• Name: 5-Amino-1,3,4-thiadiazole-2-thiol
• Synonyms: 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-mercaptothiadiazole, 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-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 180,1,3,4-Thiadiazole-2-thiol, 5-amino- (6CI,8CI), Δ2-1,3,4-Thiadiazoline-2-thiol, 5-imino- (7CI), 2-Amino-1,3,4-thiadiazol-5-thiol, 2-Amino-5-sulfanyl-1,3,4-thiadiazole, 2-Amino-5-sulfhydryl-1,3,4-thiadiazole, 2-Amino-Δ2-1,3,4-thiadiazoline-5-thione, 2-Mercapto-5-aminothiadiazole, 5-Amino-1,3,4-thiadiazole-5-thiol
• Brand: TRC

Description

Impurity Acetazolamide EP Impurity G
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);

Chemical properties

• Molecular weight: 133.19
• Formula: C₂H₃N₃S₂
• Color/Form: Neat
• InChI: InChI=1S/C2H3N3S2/c3-1-4-5-2(6)7-1/h(H2,3,4)(H,5,6)
• InChI key: InChIKey=GDGIVSREGUOIJZ-UHFFFAOYSA-N
• SMILES: N=c1[nH][nH]c(=S)s1