773868-40-9

Basic information

• Product Name: (2-(tert-butylthio)phenyl)methanol
• Synonyms: (2-(tert-butylthio)phenyl)methanol
• CAS NO: 773868-40-9
• Molecular Weight: 196.313
• Mol File: 773868-40-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2-(tert-butylthio)phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-(tert-butylthio)phenyl)methanol(773868-40-9)
• EPA Substance Registry System: (2-(tert-butylthio)phenyl)methanol(773868-40-9)

Safety Data

• Hazardous Substances Data: 773868-40-9(Hazardous Substances Data)

Upstream product

• 110-06-5 di-tert-butyl disulfide 
• 100-66-3 methoxybenzene 
• 611-74-5 N,N-dimethylbenzamide 
• 7611-60-1 2-(tert-butylthio)benzoic acid 
• 147-93-3 Thiosalicylic acid 
• 127787-04-6 N-(Bis-trimethylsilanyl-methyl)-N-methyl-benzamide 
• 65924-65-4 2-(tert-butylthio)benzaldehyde 
• 127787-14-8 N-(Bis-trimethylsilanyl-methyl)-2-tert-butylsulfanyl-N-methyl-benzamide 

Downstream Products

• 1006885-72-8 (2-(tertbutylthio)phenyl)bromomethane 
• 600735-66-8 (2-(tert-butylthio)phenyl)methanamine 
• 114772-78-0 (4′-methyl-[1,1′-biphenyl]-2-yl)methanol 
• 587-03-1 3-methylbenzyl alcohol 
• 86-26-0 2-methoxy-1,1'-biphenyl 
• 1006885-73-9 1,4-bis-(2-tert-butylsulfanyl-benzyl)-piperazine 

Relevant articles and documents

Steric hindrance effects in tripodal ligands for extraction and back-extraction of Ag+

A novel series of tripodal ligands with thiophenylether arms connected to an anchoring nitrogen has been investigated. Seven tripodal ligands were synthesized by combining methyl, isopropyl, and tert-butyl residue bearing thiophenylether sites as groups w

Nickel-catalysed Substitutions of Aryl tert-Butyl Sulfones with Organometallic Reagents: Synthesis of ortho-Substituted Unsymmetrical Biaryls

In the presence of a catalytic amount of a nickel salt, aryl tert-butyl sulfones react with aryl Grignard reagents to give biaryls.This reaction is used in conjunction with the powerful ortho-lithiation-directing ability of aryl tert-butyl sulfonyl groups to make unsymmetrical ortho-substituted biaryls.In certain cases, the substitution of an aryl alkylsulfonyl group by an organometallic reagent is possible without a transition metal catalyst.