| Weight | 130.128 g/mol |
|---|---|
| Formula | C3H2N2O2S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
1,2,3-thiadiazole-4-carboxylic acid (4100-13-4)
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- Studies on decarboxylation reactions. 3. Micellar catalysis in the decarboxylation of 5-amino-1,3,4-thiadiazole-2-carboxylic acid (Journal of Organic Chemistry, 1978)
- Studies on the oeearboxylation reactions. Note II. Kinetic study of the decarboxylation reaction of 5-amino-1,3,4-thiadiazole-2-carboxylic acid (I) to 2-amino-1,3,4-thiadiazole (III) (Journal of Heterocyclic Chemistry, 1977)
- Thiadiazoles. IV. 4-Ureido- and 4-Amino-1,2,5-thiadiazole-3-carboxylic Acid Derivatives from [1,2,5]Thiadiazolo[3,4-d]pyrimidine-5,7(4H,6H)- diones1 (Journal of Organic Chemistry, 1964)
- Thiadiazoles. II. Formation of 4-Amino-1,2,5-thiadiazole-3-carboxylic Acid and Its Derivatives by Ring-Cleavage of [1,2,5]Thiadiazolo[3,4-d]pyrimidin-7(6H)-one1,2 (Journal of Organic Chemistry, 1963)
- Photochemical conjugation of peptides to carrier proteins using 1,2,3-thiadiazole-4-carboxylic acid Immunoreactivity of free C-terminal epitope with specific antibodies (International Journal of Peptide and Protein Research, 2009)
- ChemInform Abstract: Synthesis and Antimicrobial Activity of 2Cyclopropyl[1,8]naphthyridine3carboxylic Acid (4Phenyl2thioxothiazol3yl)amides, [1,3,5]Triazine, [1,3,4]Thiadiazole2thiol, [1,2,4]Triazole3thiol and Coumarin Derivatives. (ChemInform, 2013)
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SMILESC1=C(N=NS1)C(=O)O
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InChIKeyHJZYBDPHAHGHAZ-UHFFFAOYSA-N
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