33356-45-5

Basic information

• Product Name: Benzenethiol, 2-(trimethylsilyl)-
• CAS NO: 33356-45-5
• Molecular Formula: C9H14SSi
• Molecular Weight: 182.362
• Mol File: 33356-45-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenethiol, 2-(trimethylsilyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenethiol, 2-(trimethylsilyl)-(33356-45-5)
• EPA Substance Registry System: Benzenethiol, 2-(trimethylsilyl)-(33356-45-5)

Safety Data

• Hazardous Substances Data: 33356-45-5(Hazardous Substances Data)

Upstream product

• 84998-55-0 o-Bromphenyl-trimethylsilylthioether 
• 6320-02-1 o-bromothiophenol 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 108-98-5 thiophenol 
• 20965-36-0 2-(phenylthio)tetrahydro-2H-pyran 
• 18036-83-4 o-(trimethylsilyl)phenol trimethylsilyl ether 
• 497180-95-7 O-(2-trimethylsilylphenyl)-N,N-dimethylaminothiocarbamate 
• 15288-53-6 o-(trimethylsilyl)phenol 
• 95-56-7 2-hydroxybromobenzene 
• 497180-98-0 S-(2-trimethylsilylphenyl)-N,N-dimethylaminothiocarbamate 
• 75-77-4 chloro-trimethyl-silane 
• 117526-61-1 2-(trimethylsilyl)phenyl-2-tetrahydropyranyl sulfide 

Downstream Products

• 119327-26-3 C₂₄H₃₁OPS₂Si₂ 
• 119327-15-0 2-Trimethylsilanyl-6-triphenylsilanyl-benzenethiol 
• 119327-16-1 (2-diphenylphosphanyl)-(6-trimethylsilanyl)benzenethiol 

Relevant articles and documents

Synthesis and structural Characterization of 12, an Unusual Example of a 'Paddle-Wheel' Dodecametallic Thiolate Cluster

Treatment of PF6 with the sterically-hindered thiolate ligand 2-(trimethylsilyl)benzenethiol, HSC6H4-o-SiMe3, affords red-orange crystals of 12, a dodecametallic thiolate cluster with a "paddle-wheel' C12S12 core.

Synthetic equivalents of benzenethiol and benzyl mercaptan having faint smell: Odor reducing effect of trialkylsilyl group

Syntheses and odor tests of the trialkylsilylated benzyl mercaptans and benzenethiols have revealed that the trimethylsilyl substituent on the benzene ring has a remarkable effect in reducing the foul smell of the parent benzyl mercaptan and benzenethiol.

Method of preparation of organosilyl substituted aromatic or heteroaromatic compounds

An improved method of preparing an ortho-, meta- or para-silyl aromatic or heteroaromatic compound represented by the formula STR1 wherein X is oxygen or sulfur, R1 represents the atoms necessary to complete an unsubstituted or substituted arom