41159-12-0

Basic information

• Product Name: 1,3-Dithiolane, 2-(4-bromophenyl)-2-methyl-
• CAS NO: 41159-12-0
• Molecular Formula: C10H11BrS2
• Molecular Weight: 275.233
• Mol File: 41159-12-0.mol

Chemical Properties

• CAS DataBase Reference: 1,3-Dithiolane, 2-(4-bromophenyl)-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dithiolane, 2-(4-bromophenyl)-2-methyl-(41159-12-0)
• EPA Substance Registry System: 1,3-Dithiolane, 2-(4-bromophenyl)-2-methyl-(41159-12-0)

Safety Data

• Hazardous Substances Data: 41159-12-0(Hazardous Substances Data)

Upstream product

• 99-90-1 para-bromoacetophenone 
• 540-63-6 ethane-1,2-dithiol 

Downstream Products

• 1585-07-5 1-bromo-4-ethylbenzene 
• 874884-55-6 5-(4-bromo-phenyl)-2,3-dihydro-[1,4]dithiine 
• 99-90-1 para-bromoacetophenone 

Relevant articles and documents

Selective arylthiolane deprotection by singlet oxygen: A promising tool for sensors and prodrugs

A routine thioketal protecting group reacts rapidly and selectively with singlet oxygen to reveal ketone products in good (aryl 1,3-dithiolane) to excellent (aryl 1,3-oxathiolane) yields. Arylthiolanes are stable to biologically relevant reactive oxygen species and can be used as a light-activated gating mechanism for activating fluorescent sensors or small molecule prodrugs.

Efficient method for thioacetalization of carbonyl compounds in the presence of a catalytic amount of benzyltriphenylphosphonium tribromide (BTPTB) under solvent-free conditions

A variety of carbonyl compounds have been successfully converted to the corresponding thioacetal derivatives in good to excellent yields on reaction of carbonyl compounds with 1,2-ethanedithiole, 1,3-propanedithiol, and ethylthiol in the presence of a cat

An efficient, continuous flow technique for the chemoselective synthesis of thioacetals

By optimizing a reagent's residence time within a packed-bed reactor, it is possible to overcome selectivity issues frequently encountered in stirred reaction vessels. This important feature is demonstrated for the chemoselective protection of 4-acetylben

An efficient method for thioacetalization of carbonyl compounds in the presence of a catalytic amount of benzyltriphenylphosphonium tribromide under solvent-free conditions

A variety of carbonyl compounds have been successfully converted to the corresponding thioacetal derivatives in good to excellent yields on the reaction of carbonyl compounds with 1,2-ethanedithiole, 1,3-propanedithiol, and ethanethiol in the presence of

A rapid and efficient method for 1,3-dithiolane synthesis

A mild, efficient and solvent-free protocol for conversion of aldehydes and ketones into their corresponding 1,3-dithiolanes using 1,2-ethanedithiol in the presence of a catalytic amount of SnCl2·2H2O is reported.

A simple and efficient heterogeneous procedure for thioacetalization of aldehydes and ketones

A new procedure for the protection of aldehydes and ketones as thioacetals promoted by catalytic amount of p-toluene-sulfonic acid and silica gel has been developed. This procedure offers versatility, short reaction time, excellent yield, good selectivity