3492-64-6

Basic information

• Product Name: BenzeneMethanethiol, sodiuM salt
• Synonyms: BenzeneMethanethiol, sodiuM salt
• CAS NO: 3492-64-6
• Molecular Formula: C₇H₇NaS
• Molecular Weight: 146.18525
• EINECS: -0
• Mol File: 3492-64-6.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 181.1°Cat760mmHg
• Flash Point: 71.1°C
• Appearance: /
• Density: 0.913g/cm³
• CAS DataBase Reference: BenzeneMethanethiol, sodiuM salt(CAS DataBase Reference)
• NIST Chemistry Reference: BenzeneMethanethiol, sodiuM salt(3492-64-6)
• EPA Substance Registry System: BenzeneMethanethiol, sodiuM salt(3492-64-6)

Safety Data

• Hazardous Substances Data: 3492-64-6(Hazardous Substances Data)

Usage

Benzene

widely used industrial chemical, colorless, flammable liquid with sweet, aromatic odor

Methanethiol

volatile organic compound used as chemical intermediate and in industrial product production
Used in industrial and chemical processes, pharmaceutical and agrochemical production
Important in synthesis of organic compounds

Upstream product

• 100-53-8 phenylmethanethiol 
• 7440-23-5 sodium 
• 216979-79-2 (2,9-dimethylphenanthroline) zinc bis(benzylmercaptonate) 
• 42254-28-4 disodium p-xylene-α,α'-dithiolate 

Downstream Products

• 150-60-7 dibenzyl disulphide 
• 10606-38-9 tris(phenylmethylthio)methane 
• 1631-59-0 1,3-bis-benzylsulfanyl-propan-2-ol 
• 102736-26-5 3-benzylsulfanyl-trans-crotonic acid methyl ester 
• 33741-26-3 3-benzylsulfanyl-trans-crotonic acid ethyl ester 
• 6304-94-5 benzylmercaptoacetaldehyde dimethyl acetal 
• 105449-77-2 2-benzylsulfanyl-2-methylpropanal 
• 98176-50-2 7-(2-benzylmercapto-ethyl)-1,3-dimethyl-3,7-dihydro-purine-2,6-dione 
• 724-34-5 6-benzylthiopurine 
• 26902-03-4 3-(benzylthio)propan-1-ol 
• 10230-69-0 benzylthioacetone 
• 6937-97-9 allyl(benzyl)sulfide 
• 195526-18-2 1,2-bis-(benzylsulfanyl-methyl)-benzene 
• 103479-95-4 rac-19-acetyl-15-benzylmercapto-10-oxo-8,11,12,13,14,15-hexadehydro-de-F,G-strychnidine-14-carboxylic acid methyl ester 

Relevant articles and documents

Practical and efficient recyclable oxidative system for the preparation of symmetrical disulfides under aerobic conditions

An efficient and practical oxidative coupling of thiols to symmetrical disulfides is developed at room temperature under aerobic conditions. The commercially available sodium methoxide solution 30 wt. % in methanol together with the air was used as a retrievable promoter system and green oxidant, respectively, for the preparation of symmetrical disulfides. The desired products were obtained in good to high yields by an economical procedure. No overoxidation of the symmetrical disulfides was observed, and various functional groups were well tolerated in the current protocol. Moreover, the new reagent reduces the generation of hazardous waste due to its high reusability. The reaction proceeded in the absence of light, and it was not inhibited by TEMPO. Also, the low yield of TEMPO-benzyl thiol adduct was detected under these conditions. Based on our experiments, a possible mechanism was proposed in the absence and presence of TEMPO.

SYNTHETIC VACCINES AGAINST STREPTOCOCCUS PNEUMONIAE TYPE 1

The present invention relates to the total synthesis of saccharide structures contained in the capsular polysaccharide of Streptococcus pneumoniae type 1, to glycoconjugates containing said saccharide structures obtained by total synthesis and to use of s

METHODS OF FORMING SINGLE SOURCE PRECURSORS, METHODS OF FORMING POLYMERIC SINGLE SOURCE PRECURSORS, AND SINGLE SOURCE PRECURSORS AND INTERMEDIATE PRODUCTS FORMED BY SUCH METHODS

Methods of forming single source precursors (SSPs) include forming intermediate products having the empirical formula ?{L2N(μ-X)2M′X2}2, and reacting MER with the intermediate products to form SSPs of the formula L2N(μ-ER)2M′(ER)2, wherein L is a Lewis base, M is a Group IA atom, N is a Group IB atom, M′ is a Group IIIB atom, each E is a Group VIB atom, each X is a Group VIIA atom or a nitrate group, and each R group is an alkyl, aryl, vinyl, (per)fluoro alkyl, (per)fluoro aryl, silane, or carbamato group. Methods of forming polymeric or copolymeric SSPs include reacting at least one of HE1R1E1H and MER with one or more substances having the empirical formula L2N(μ-ER)2M′(ER)2 or L2N(μ-X)2M′(X)2 to form a polymeric or copolymeric SSP. New SSPs and intermediate products are formed by such methods.