34832-35-4

Basic information

• Product Name: SODIUMTHIOLACETATE
• Synonyms: SODIUMTHIOLACETATE;Thioacetic acid sodium salt
• CAS NO: 34832-35-4
• Molecular Formula: C₂H₃OS*Na
• Molecular Weight: 0
• Mol File: 34832-35-4.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 93°Cat760mmHg
• Flash Point: 11.1°C
• Appearance: /
• Density: 1.046g/cm³
• Vapor Pressure: 4.3mmHg at 25°C
• CAS DataBase Reference: SODIUMTHIOLACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: SODIUMTHIOLACETATE(34832-35-4)
• EPA Substance Registry System: SODIUMTHIOLACETATE(34832-35-4)

Safety Data

• Hazardous Substances Data: 34832-35-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C2H4OS.Na/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

Upstream product

• 507-09-5 tiolacetic acid 
• 18773-93-8 1-acetyl-1H-benzotriazole 

Downstream Products

• 6633-90-5 1,4-bis-acetylsulfanyl-butane 
• 72-89-9 acetylcoenzyme A 
• 62672-40-6 1-acetyl-6-nitro-3-phenyl-1H-benzo[1,3,4]thiadiazine 
• 80365-94-2 (Z)-7-[(1S,2R,4S,6R)-2-Acetylsulfanyl-4-(tetrahydro-pyran-2-yloxy)-6-(tetrahydro-pyran-2-yloxymethyl)-cyclohexyl]-hept-5-enoic acid methyl ester 
• 84234-92-4 1-<3-(4-bromobenzoyl)-4-(acetylthio)butyryl>-L-proline methyl ester 
• 89664-76-6 α-(acetylthio)-4-bromoacetophenone 
• 57359-76-9 (2R)-2-(acetylthio)-3-phenylpropanoic acid 
• 76932-17-7 (S)-2-acetylthio-3-phenylpropanoic acid 
• 194656-62-7 1-{3,5-Di-O-benzoyl-2-deoxy-4-C-[(acetylsulfanyl)methyl]-β-D-erythro-pentofuranosyl}uracil 
• 197566-25-9 Thioacetic acid S-{1-[((E)-propenyl)sulfanyl]-propyl} ester 
• 88031-93-0 2,3-dimercaptopropane-1-sulphonic acid 
• 353238-14-9 S-[2-(1-sec-butyl-2,2-difluorovinyl)benzyl] thioacetate 
• 353238-13-8 S-[2-(1-butyl-2,2-difluorovinyl)benzyl] thioacetate 
• 999-90-6 S-tert-butyl thioacetate 

Relevant articles and documents

Preparation method of sodium thioacetate and method for preparing thiolactone by using sodium thioacetate

The invention relates to the field of organic chemistry, and discloses a preparation method of sodium thioacetate and a method for preparing thiolactone from sodium thioacetate, which are characterized in that the method comprises the following steps: in the presence of a first solvent, reacting RONa with thioacetic acid; wherein R is an alkyl group of C1 to C4, preferably an alkyl group of C1 toC2. The method has the advantages of simple process, cheap and easily available raw materials and high product yield, and provides convenience for industrial production of sodium thioacetate. The thiolactone prepared from the sodium thioacetate prepared by the method has the advantages of high reaction yield, few side reactions and high product purity.

Amine Induced Retardation of the Radical-Mediated Thiol-Ene Reaction via the Formation of Metastable Disulfide Radical Anions

The effect of amines on the kinetics and efficacy of radical-mediated thiol-ene coupling (TEC) reactions was investigated. By varying the thiol reactant and amine additive, it was shown that amines retard thiyl radical-mediated reactions when the amine is

Antibacterial β-lactam compounds

Novel β-lactam compounds classified into penem compounds, a process for preparing the same and use of such β-lactam compounds are disclosed. These β-lactam compounds exhibit excellent antimicrobial activities useful as pharmaceuticals or they are important intermediates for the synthesis of compounds having antimicrobial activities.