442850-92-2

Basic information

• Product Name: Carbamic acid, (2-ethenylphenyl)-, 1,1-dimethylethyl ester (9CI)
• Synonyms: Carbamic acid, (2-ethenylphenyl)-, 1,1-dimethylethyl ester (9CI)
• CAS NO: 442850-92-2
• Molecular Formula: C₁₃H₁₇NO₂
• Molecular Weight: 219.27958
• Product Categories: N-BOC
• Mol File: 442850-92-2.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Carbamic acid, (2-ethenylphenyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (2-ethenylphenyl)-, 1,1-dimethylethyl ester (9CI)(442850-92-2)
• EPA Substance Registry System: Carbamic acid, (2-ethenylphenyl)-, 1,1-dimethylethyl ester (9CI)(442850-92-2)

Safety Data

• Hazardous Substances Data: 442850-92-2(Hazardous Substances Data)

Upstream product

• 78839-75-5 2-bromo-N-(tert-butoxycarbonyl)aniline 
• 92988-08-4 trivinylboroxin 
• 27326-43-8 2-vinylbenzoic acid 
• 75-65-0 tert-butyl alcohol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 3867-18-3 2-vinylaniline 
• 615-36-1 2-bromoaniline 
• 880384-47-4 di-tert-butyl (2-bromophenyl)carbamate 
• 4248-19-5 tert-butyl carbazate 
• 105952-36-1 1-iodo-2-(2-iodoethyl)-benzene 
• 5339-85-5 2-aminophenethyl alcohol 
• 7486-35-3 tri-n-butyl(vinyl)tin 

Downstream Products

• 686775-90-6 tert-butyl benzyl(2-vinylphenyl)carbamate 
• 686776-03-4 tert-butyl (4-methylphenyl)sulfonyl(2-vinylphenyl)carbamate 
• 894810-56-1 allyl-(2-vinyl-phenyl)-carbamic acid tert-butyl ester 
• 34943-91-4 1-benzyl-3-methyl-1,3-dihydro-2H-indol-2-one 

Relevant articles and documents

Ruthenium Amide Complexes – Synthesis and Catalytic Activity in Olefin Metathesis and in Ring-Opening Polymerisation

A set of olefin metathesis catalysts bearing a ruthenium amide moiety was synthesised. In the ruthenium amide form these complexes exhibit very low activity in standard metathesis reactions. However, a dramatic increase of activity was observed upon in si

Thiol-ene/oxidation tandem reaction under visible light photocatalysis: Synthesis of alkyl sulfoxides

The photocatalyzed synthesis of sulfoxides from alkenes and thiols has been carried out using Eosin Y. This is a metal-free method which uses a low catalyst loading, atmospheric oxygen as the oxidant, and visible light conditions (green light). A mechanism has been proposed that is consistent with the experimental results.

Synthesis of indolines via a domino Cu-catalyzed amidation/cyclization reaction

(Chemical Equation Presented) A highly efficient one-pot procedure for the synthesis of indolines and their homologues based on a domino Cu-catalyzed amidation/nucleophilic substitution reaction has been developed. Substituted 2-iodophenethyl mesylates and related compounds afforded the corresponding products in excellent yields. No erosion of optical purity was observed when transforming enantiomerically pure mesylates under the reaction conditions.