28519-31-5

Basic information

• Product Name: 1-butan-2-yloxysulfonothioyl-4-methyl-benzene
• Synonyms: 1-butan-2-yloxysulfonothioyl-4-methyl-benzene;4-Methylbenzene-1-thiosulfonic acid S-butyl ester;4-Methylbenzenesulfonothioic acid S-butyl ester
• CAS NO: 28519-31-5
• Molecular Formula: C₁₁H₁₆O₂S₂
• Molecular Weight: 0
• Mol File: 28519-31-5.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 326.8°Cat760mmHg
• Flash Point: 151.4°C
• Appearance: /
• Density: 1.154g/cm³
• Vapor Pressure: 0.000402mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: 1-butan-2-yloxysulfonothioyl-4-methyl-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-butan-2-yloxysulfonothioyl-4-methyl-benzene(28519-31-5)
• EPA Substance Registry System: 1-butan-2-yloxysulfonothioyl-4-methyl-benzene(28519-31-5)

Safety Data

• Hazardous Substances Data: 28519-31-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H16O2S2/c1-4-10(3)13-15(12,14)11-7-5-9(2)6-8-11/h5-8,10H,4H2,1-3H3

Upstream product

• 150-50-5 merphos 
• 104-15-4 toluene-4-sulfonic acid 
• 629-45-8 dibutyl disulfide 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 109-79-5 n-butanethiol 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 542-69-8 1-iodo-butane 
• 3753-27-3 sodium 4-methylbenzenesulfonothioate 
• 78-48-8 S,S,S-tributylphosphorotrithioate 
• 28519-50-8 potassium thiotosylate 
• 536-57-2 p-toluene sulfinic acid 
• 109-65-9 1-bromo-butane 

Downstream Products

• 69187-12-8 4-methylphenyl n-butyl disulfide 
• 37456-99-8 2-(Butylthio)cyclohexanon 

Relevant articles and documents

Ammonium iodide-mediated electrosynthesis of unsymmetrical thiosulfonates from arenesulfonohydrazides and thiols

Unsymmetrical thiosulfonates were synthesized from thiols and arenesulfonohydrazides by their electrolysis in undivided cell equipped with graphite anode and stainless steel cathode under high current density applying NH4I both as a redox catal

Oxidative coupling of dichalcogenides with sodium sulfinates via copper-catalyzed cleavage of s-s and se-se bonds

A copper-catalyzed sulfonylation of disulfides was achieved using sodium sulfinates in air. The reaction formed various sulfur-sulfone bonds efficiently and afforded thiosulfonates in good yields. Selenosulfonates could also be prepared with this procedure. Furthermore, both chalcogenide groups on the dichalcogenides were available in these reactions.

MUTILIN DERIVATIVE HAVING HETEROCYCLIC AROMATIC RING CARBOXYLIC ACID STRUCTURE IN SUBSTITUENT AT 14-POSITION

To provide a novel mutilin derivative having a substitution at the 14-position, which is a novel mutilin analogue exhibiting a potent and broad antimicrobial action against Gram-positive bacteria and Gram-negative bacteria including various drug-resistant bacteria, and which is expected to be useful as an agent for treating infectious diseases. A mutilin derivative represented by the following general formula (1): or a pharmaceutically acceptable addition salt thereof.