83126-01-6

Basic information

• Product Name: Benzene, [(1E)-3-bromo-2-methyl-1-propenyl]-
• CAS NO: 83126-01-6
• Molecular Formula: C10H11Br
• Molecular Weight: 211.101
• Mol File: 83126-01-6.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzene, [(1E)-3-bromo-2-methyl-1-propenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(1E)-3-bromo-2-methyl-1-propenyl]-(83126-01-6)
• EPA Substance Registry System: Benzene, [(1E)-3-bromo-2-methyl-1-propenyl]-(83126-01-6)

Safety Data

• Hazardous Substances Data: 83126-01-6(Hazardous Substances Data)

Upstream product

• 10409-54-8 2-bromo-2-methyl-1-phenyl-propan-1-one 
• 555-31-7 aluminum isopropoxide 
• 1504-55-8 (E)-3-phenyl-2-methyl-2-propenol 
• 1504-55-8 2-methyl-3-phenylprop-2-en-1-ol 

Downstream Products

• 83126-03-8 (E)-(2-Methyl-3-phenyl-2-propenyl)malonsaeure-diethylester 
• 54860-39-8 (E)-3-Methyl-4-phenyl-3-butensaeure-methylester 
• 83126-02-7 (E)-3-methyl-4-phenylbut-3-ene-1-ol 
• 57919-03-6 (E)-4-Methyl-5-phenyl-4-penten-1-ol 
• 83126-04-9 (4E)-4-methyl-5-phenylpent-4-enoic acid 
• 3290-53-7 2-methyl-1-phenyl-2-propene 

Relevant articles and documents

MICROBIOCIDAL QUINOLINE DIHYDRO-(THIAZINE)OXAZINE DERIVATIVES

Compounds of formula (I), wherein the subsitiuents are as defined in claim 1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling infestation of plants, harvested food crops, seeds or non-living materials by phytopathogenic microorganisms, in particular fungi.

Asymmetric Synthesis of Cα-Substituted Prolines through Curtin–Hammett-Controlled Diastereoselective N-Alkylation

Asymmetric synthesis of α-substituted proline derivatives has been accomplished by an efficient chirality-transfer method. High diastereoselectivity of the N-alkylation of the proline ester (C→N chirality transfer) was achieved when a 2,3-disubstituted be

Palladium-catalyzed oxidative arylacetoxylation of alkenes: Synthesis of indole and indoline derivatives

A method for the oxidative arylacetoxylation of alkenes has been developed to synthesize indole and indoline derivatives from readily accessible substrates. The cinnamyl tethered anilines with picolinamide as a directing group provided 3-substituted indoles via intramolecular oxidative arylacetoxylation, and the 2-methyl substituted cinnamyl anilines furnished indoline derivatives with 3-position quaternary stereocenters in good to excellent yields via sequential intramolecular oxidative arylacetoxylation, hydrolysis and oxidation steps.