121392-35-6

Basic information

• Product Name: S-butyl 4-bromothiophenol
• Synonyms: (4-Bromophenyl)(butyl)sulfane;1-Bromo-4-butylthiobenzene;4-bromophenyl butyl sulfide;S-butyl 4-bromothiophenol
• CAS NO: 121392-35-6
• Molecular Formula: C₁₀H₁₃BrS
• Molecular Weight: 245.17922
• Mol File: 121392-35-6.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: S-butyl 4-bromothiophenol(CAS DataBase Reference)
• NIST Chemistry Reference: S-butyl 4-bromothiophenol(121392-35-6)
• EPA Substance Registry System: S-butyl 4-bromothiophenol(121392-35-6)

Safety Data

• Hazardous Substances Data: 121392-35-6(Hazardous Substances Data)

Usage

General Description

S-butyl 4-bromothiophenol is a chemical compound with the molecular formula C10H11BrOS. It consists of a butyl group attached to a 4-bromothiophenol core, which contains a five-membered ring with a sulfur atom and a bromine atom. S-butyl 4-bromothiophenol is commonly used as a building block in the synthesis of organic compounds and pharmaceutical drugs due to its unique structure and reactivity. It is also utilized in the field of materials science for its potential applications in the development of new materials with specific properties. S-butyl 4-bromothiophenol may also have potential uses in the field of agrochemicals and as a precursor in the production of various industrial chemicals.

Upstream product

• 109-65-9 1-bromo-butane 
• 106-53-6 para-bromobenzenethiol 
• 1207372-98-2 butyl 2-[2-(4-methoxyphenyl)ethynyl]benzoate 
• 629-45-8 dibutyl disulfide 
• 589-87-7 1,4-bromoiodobenzene 
• 542-69-8 1-iodo-butane 
• 109-79-5 n-butanethiol 
• 1126-80-3 (n-butylthio)benzene 

Downstream Products

• 3226-41-3 4-bromobenzenediazonium tetrafluoroborate 
• 151588-38-4 (4-(butylthio)phenyl)boronic acid 
• 1415309-92-0 C₁₆H₂₅BO₂S 
• 1415309-78-2 C₁₄H₁₇N₃OS 
• 1373154-07-4 (R)-1-bromo-4-(butylsulfinyl)benzene 
• 403793-28-2 (4-bromo-phenyl)-butyl sulfone 
• 1210812-41-1 2-(4-butylsulfanylphenylsulfanyl)phenylamine 
• 294895-76-4 1-(2-aminopyrimidin-5-yl)-2-(4-butylsulfanylphenyl)ethyne 
• 294895-71-9 3-(4-butylsulfanylphenyl)propiolic acid 
• 223399-81-3 1-(4-aminophenyl)-2-(4-butylsulfanylphenyl)ethyne 
• 294895-70-8 4-butylsulfanylphenylethyne 
• 294895-69-5 1-butylsulfanyl-4-(3-hydroxy-3-methylbut-1-ynyl)benzene 

Relevant articles and documents

Alkoxylation reactions of aryl halides catalyzed by magnetic copper ferrite

Copper ferrite (CuFe2O4), which is easy-made, air-stable, low cost, easy separable, and regenerable, was applied as catalyst in an efficient method for C-O coupling reactions between various kinds of unactivated alkyl alcohols and aryl halides. This method only adopts 2.5% mol CuFe2O4 catalyst and selectively proceeds to C-O bond formation even sensitive substituents exist in the system.

Recyclable heterogeneous supported copper-catalyzed coupling of thiols with aryl halides: base-controlled differential arylthiolation of bromoiodobenzenes

Alumina-supported copper sulfate efficiently catalyzes the 5-arylation of aromatic, heteroaromatic and aliphatic thiols with aryl as well as heteroaryl halides under aerobic, ligand-free conditions. This protocol provides an easy access to a variety of thioethers as well as unsymmetrical bis-thioethers by base-controlled differential coupling of thiols with iodo- and bromo-substituents in an aromatic halide. The catalyst is inexpensive, non-air sensitive, environmentally friendly and recyclable.

A mild and efficient copper-catalyzed coupling of aryl iodides and thiols using an oxime-phosphine oxide ligand

A mild and efficient copper-catalyzed system for the coupling of aryl iodides and thiols was developed using a readily prepared and highly stable oxime-phosphine oxide ligand. Good to excellent yields were obtained.