849589-04-4

Basic information

• Product Name: Benzeneacetic acid, 3,4-dichloro-a-cyano-, Methyl ester
• Synonyms: Benzeneacetic acid, 3,4-dichloro-a-cyano-, Methyl ester
• CAS NO: 849589-04-4
• Molecular Formula: C₁₀H₇Cl₂NO₂
• Molecular Weight: 244.07408
• Mol File: 849589-04-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzeneacetic acid, 3,4-dichloro-a-cyano-, Methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, 3,4-dichloro-a-cyano-, Methyl ester(849589-04-4)
• EPA Substance Registry System: Benzeneacetic acid, 3,4-dichloro-a-cyano-, Methyl ester(849589-04-4)

Safety Data

• Hazardous Substances Data: 849589-04-4(Hazardous Substances Data)

Upstream product

• 616-38-6 carbonic acid dimethyl ester 
• 3218-49-3 3,4-dichloro-benzeneacetonitrile 
• 75-86-5 2-hydroxy-2-methylpropanenitrile 
• 393164-93-7 methyl 2-diazo-2-(3,4-dichlorophenyl)acetate 

Downstream Products

• 852103-39-0 cyano-(3,4)-dichlorophenyl acetic acid isopropyl ester 
• 1006612-79-8 dimethyl 2-cyano-2-(3,4-dichlorophenyl)pentanedioate 

Relevant articles and documents

Construction of quaternary carbon stereocentres: Catalytic enantioselective allylation assisted by a bimetallic catalytic system

The asymmetric allylic alkylation of prochiral aryl cyano esters has been carried out in the presence of a bi-component catalytic system containing a palladium and a rhodium complex modified by phosphorus containing chiral auxiliaries. The allyl derivativ

Highly selective preparation of a chiral quaternary allyl aryl piperidinedione by palladium-catalyzed asymmetric allylation under solid-liquid phase-transfer catalysis

The combination of a chiral palladium catalyst and a solid-liquid phase-transfer catalyst provides an effective method for the chemo- and enantioselective preparation of the chiral quaternary center of an allyl aryl piperidinedione. Wiley-VCH Verlag GmbH