135883-45-3

Basic information

• Product Name: Benzene, 1-[(1,1-dimethylethyl)thio]-4-ethynyl-
• Synonyms: 1-tert-Butylsulfanyl-4-ethynyl-benzene;4-ethynylphenyl tert-butyl sulfide;tert-butyl(4-ethynylphenyl)sulfane;1-tert-butylthio-4-ethynylbenzene;1-tert-butylsulfanyl-4-ethynylbenzene
• CAS NO: 135883-45-3
• Molecular Formula: C12H14S
• Molecular Weight: 190.309
• Mol File: 135883-45-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[(1,1-dimethylethyl)thio]-4-ethynyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[(1,1-dimethylethyl)thio]-4-ethynyl-(135883-45-3)
• EPA Substance Registry System: Benzene, 1-[(1,1-dimethylethyl)thio]-4-ethynyl-(135883-45-3)

Safety Data

• Hazardous Substances Data: 135883-45-3(Hazardous Substances Data)

Upstream product

• 106-53-6 para-bromobenzenethiol 
• 65688-19-9 1-(tert-butylsulfanyl)-4-iodobenzene 
• 352-34-1 4-fluoro-1-iodobenzene 
• 25752-90-3 tert-butyl 4-bromophenyl sulfide 
• 795274-48-5 1-tert-butylsulfanyl-4-(2'-triisopropylsilylethynyl)-benzene 
• 135883-41-9 1-(tert-butylsulfanyl)-4-(trimethylsilylethynyl)benzene 

Downstream Products

• 894351-56-5 2,6-bis((4-(tert-butylthio)phenyl)ethynyl)anthracene-9,10-dione 
• 1402451-60-8 1,3-bis[(4-tert-butylthiophenyl)ethynyl]azulene 
• 1364344-62-6 2,6-bis[(4-acetylthiophenyl)ethynyl]naphthalene 

Relevant articles and documents

Monitoring Solid-Phase Reactions in Self-Assembled Monolayers by Surface-Enhanced Raman Spectroscopy

Nanopatterned surfaces enhance incident electromagnetic radiation and thereby enable the detection and characterization of self-assembled monolayers (SAMs), for instance in surface-enhanced Raman spectroscopy (SERS). Herein, Au nanohole arrays, developed

Bismuth(III)-Promoted Acetylation of Thioethers into Thioacetates

The thioacetate group is extensively employed as an anchoring group for attachment of molecules onto gold surfaces or between electrodes in molecular electronics. On account of its ready hydrolysis, it is often incorporated in the last step of a synthetic

Formation of high-quality self-assembled monolayers of conjugated dithiols on gold: Base matters

This Article reports a systematic study on the formation of self-assembled monolayers (SAMs) of conjugated molecules for molecular electronic (ME) devices. We monitored the deprotection reaction of acetyl protected dithiols of oligophenylene ethynylenes (