CAS 32873-56-6

2-Acetylamino-5-mercapto-1,3,4-thiadiazole

Description:

2-Acetylamino-5-mercapto-1,3,4-thiadiazole is a heterocyclic compound characterized by the presence of a thiadiazole ring, which contains both sulfur and nitrogen atoms. This compound features an acetylamino group and a mercapto group, contributing to its reactivity and potential biological activity. The thiadiazole structure is known for its diverse applications in pharmaceuticals, agrochemicals, and materials science due to its ability to form coordination complexes and its potential as a bioactive scaffold. The mercapto group (-SH) can participate in redox reactions and may enhance the compound's antioxidant properties. Additionally, the acetylamino group can influence solubility and interaction with biological targets. Overall, 2-Acetylamino-5-mercapto-1,3,4-thiadiazole is of interest for its potential applications in medicinal chemistry and as a building block for the synthesis of more complex molecules. Its unique structural features make it a subject of study for various chemical and biological investigations.

Formula: C₄H₅N₃OS₂

InChI: InChI=1/C4H5N3OS2/c1-2(8)5-3-6-7-4(9)10-3/h1H3,(H,7,9)(H,5,6,8)

InChI key: InChIKey=DWSMAMSVZRCQMP-UHFFFAOYSA-N

SMILES: N(C(C)=O)C=1SC(=S)NN1

Synonyms:

• 1,3,4-Thiadiazole-2-thiol, 5-acetamido-
• 2-(Acetylamino)-1,3,4-thiadiazol-5-mercaptan
• 2-Acetylamino-5-mercapto-1,3,4-thiadiazole
• 5-Acetylamino-1,3,4-thiadiazoline-2-thione
• AMT
• Acetamide, N-(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)-
• Acetamide, N-(5-mercapto-1,3,4-thiadiazol-2-yl)-
• N-(4,5-Dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)acetamide
• N-(5-thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)acetamide
• NSC 97893
• 2-Acetamido-5-mercapto-1,3,4-thiadiazole
• EAMTD
• ACETYLAMINE(2-)-5-MERCAPTO-1,3,4-THIADAZOLE
• 5-(Acetylamino)-1,3,4-thiadiazole-2-thiol
• EAMTD:2-ACETYLAMINO-5-MERCAPTO-1,3,4-THIADIAZOLE
• 5-(Acetylamino)-2,3-dihydro-1,3,4-thiadiazole-2-thione

2-Acetylamino-5-mercapto-1,3,4-thiadiazole

CAS: 32873-56-6

Formula: C₄H₅N₃OS₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 175.2320

Ref: IN-DA00BXFB

Acetazolamide EP Impurity C

CAS: 32873-56-6

Formula: C₄H₅N₃OS₂

Color and Shape: White To Off-White Solid

Molecular weight: 175.22

Ref: 4Z-A-356

N-(5-Thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)acetamide

CAS: 32873-56-6

N-(5-Thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)acetamide

Purity: 98%

Molecular weight: 175.232g/mol

Ref: 54-OR96516

Acetazolamide EP Impurity C

CAS: 32873-56-6

Formula: C₄H₅N₃OS₂

Molecular weight: 175.23

Ref: ST-EA-CP-A6003

2-Acetamido-5-mercapto-1,3,4-thiadiazole

Controlled Product

CAS: 32873-56-6

Impurity Acetazolamide EP Impurity C
Applications Acetazolamide intermediate. Acetazolamide EP Impurity C
References Almajan, G., et al.: Bioorg. Med. Chem. Lett., 15, 2347 (2005), Talath, S., et al.: Eur. J. Med. Chem., 41, 918 (2006), Srinivasu, P., et al.: J. Pharm. Biomed. Anal., 52, 142 (2010),

Formula: C₄H₅N₃OS₂

Color and Shape: Neat

Molecular weight: 175.23

Ref: TR-A168105

N-(5-sulfanylidene-4,5-dihydro-1,3,4-thiadiazol-2-yl)acetamide

CAS: 32873-56-6

Formula: C₄H₅N₃OS₂

Purity: 98%

Molecular weight: 175.22

Ref: 10-F358316

2-Acetamido-5-mercapto-1,3,4-thiadiazole

CAS: 32873-56-6

2-Acetamido-5-mercapto-1,3,4-thiadiazole is a fluxional molecule that undergoes a transition from an uncharged state to an ionic state. This compound has been used as a sensor for the detection of metal ions. The electrochemical impedance spectroscopy technique was used to study the interaction between 2-acetamido-5-mercapto-1,3,4-thiadiazole and polymeric matrix coatings. These coatings are designed to prevent corrosion by forming a barrier on metallic surfaces. 2-Acetamido-5-mercapto-1,3,4-thiadiazole was also shown to be a potent ligand for metal ions and has been used in techniques such as ionophores.

Formula: C₄H₅N₃OS₂

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 175.23 g/mol

Ref: 3D-FA16934