758-08-7

Basic information

• Product Name: 2-MERCAPTOACETAMIDE
• Synonyms: 2-mercapto-acetamid;2-mercapto-acetamidcrude;alpha-mercaptoacetamide;crudethioglycolamide;mercaptoacetamide;thioglycolamide;thioglycolamide(crude);2-MERCAPTOACETAMIDE
• CAS NO: 758-08-7
• Molecular Formula: C₂H₅NOS
• Molecular Weight: 91.13
• Product Categories: Aliphatics
• Mol File: 758-08-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 157.5-158.5 °C
• Boiling Point: 279.3°C at 760 mmHg
• Flash Point: 12
• Appearance: /
• Density: 1.192g/cm³
• Vapor Pressure: 0.00405mmHg at 25°C
• Refractive Index: 1.508
• PKA: 8.34±0.10(Predicted)
• CAS DataBase Reference: 2-MERCAPTOACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-MERCAPTOACETAMIDE(758-08-7)
• EPA Substance Registry System: 2-MERCAPTOACETAMIDE(758-08-7)

Safety Data

• Hazard Codes: C,F,T
• Statements: 11-20/21/22
• Safety Statements: 16-26-36/37/39
• RIDADR: 1993
• Hazardous Substances Data: 758-08-7(Hazardous Substances Data)

Usage

General Description

2-Mercaptoacetamide is a chemical compound with the formula C2H5NOS. It is a thiol derivative of acetamide and contains a sulfhydryl group, which makes it a versatile compound for various chemical reactions. 2-Mercaptoacetamide is commonly used as a chelating agent, especially in metal ions binding and removal. It is also used as a precursor in the preparation of pharmaceuticals and other organic compounds. Additionally, 2-Mercaptoacetamide has antimicrobial properties, making it useful in the production of antifungal and antibacterial agents. Its ability to form complexes with metal ions also makes it valuable in analytical chemistry and biochemical studies.

InChI:InChI=1/C2H5NOS/c3-2(4)1-5/h5H,1H2,(H2,3,4)

Upstream product

• 79-07-2 Chloroacetamide 
• 75032-76-7 4-thioxo-3-oxa-5-thia-heptanedioic acid-7-amide 
• 68-11-1 mercaptoacetic acid 
• 140-89-6 potassium ethyl xanthogenate 
• 79-04-9 chloroacetyl chloride 
• 623-51-8 ethyl 2-sulfanylacetate 
• 2365-48-2 Methyl thioglycolate 
• 19788-48-8 2-methoxyethyl 2-mercaptoacetate 

Downstream Products

• 105855-53-6 2,2-diphenyl-thiazolidin-4-one 
• 2281-74-5 4-oxothiazolidine 
• 133401-89-5 dimethylarsinomercapto-acetic acid amide 
• 64057-55-2 NSC 28727 
• 6032-95-7 methyl 6-(4-oxothiazolidin-2-yl)hexanoate 
• 6603-40-3 DL-Mycobacidinethylester 
• 99072-38-5 (4-nitro-phenacylmercapto)-acetic acid amide 
• 799255-17-7 (α-hydroxy-benzylsulfanyl)-acetic acid amide 
• 55557-48-7 3-Amino-2-carboxamidothieno<2,3-b>pyridine 
• 67795-42-0 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxamide 
• 18504-86-4 2H-pyrido<4,3-b><1,4>thiazin-3(4H)-one 
• 147123-47-5 3-aminothiophene-2-carboxamide 

Relevant articles and documents

Design, synthesis, and biological evaluation of novel derivatives of dithiodiglycolic acid prepared via oxidative coupling of thiols

Human thioredoxin reductase 1 (TrxR1) is a selenocysteine-containing enzyme which plays a crucial role in regulating numerous redox signalling pathways within the cell. While its functioning is important in all cells, levels of TrxR1 expression are higher

Corresponding amine nitrile and method of manufacturing thereof

The invention relates to a manufacturing method of nitrile. Compared with the prior art, the manufacturing method has the characteristics of significantly reduced using amount of an ammonia source, low environmental pressure, low energy consumption, low production cost, high purity and yield of a nitrile product and the like, and nitrile with a more complex structure can be obtained. The invention also relates to a method for manufacturing corresponding amine from nitrile.

NOVEL THIAZINE OR PYRAZINE DERIVATIVES

An object of the present invention is to synthesize novel compounds having 3-oxo-3, 4-dihydro-2H-1, 4-thiazine or 2-oxo-1, 2, 3, 4-tetrahydropyrazine as a main skeleton. The present invention relates to compounds represented by the following general formula [I] and salts thereof. In the formula, X is S or R6-(A2)n-N, R1 and R2 are H, alkyl, cycloalkyl or aryl, R3 and R4 are H, alkyl, cycloalkyl, aryl or aromatic heterocycles, R5 is H, alkyl, cycloalkyl, aryl or -A3-A4-R7, R6 is H, alkyl, cycloalkyl, OH, alkoxy, aryl, aryloxy or an aromatic heterocycle, R7 is H, alkyl, OH, alkoxy, aryl, aryloxy, amino, alkylamino, arylamino, an aromatic heterocycle or a nonaromatic heterocycle, A1 is alkylene, A2 is carbonyl or sulfonyl, A3 is alkylene, and A4 is carbonyl or oxalyl.