70729-31-6

Basic information

• Product Name: 2-chloro-2-phenylpropanal
• CAS NO: 70729-31-6
• Molecular Weight: 168.623
• Mol File: 70729-31-6.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 2-chloro-2-phenylpropanal(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-2-phenylpropanal(70729-31-6)
• EPA Substance Registry System: 2-chloro-2-phenylpropanal(70729-31-6)

Safety Data

• Hazardous Substances Data: 70729-31-6(Hazardous Substances Data)

Upstream product

• 51673-52-0 N-chloro-N'-tosylbenzamidine 
• 24401-44-3 β-Piperidino-α-methyl styrene 
• 113676-38-3 N-chloro-N'-(4-nitrobenzenesulfonyl)-benzamidine 
• 19733-68-7 N-chloropyrrolidine 
• 34713-70-7 2-Phenylpropanal 
• 2156-71-0 N-chloropiperidine 
• 107116-39-2 Pentachloro<2-phenyl-1-(1-pyridinio)propoxy>antiomonat 
• 121034-41-1 2-(4-Chloro-phenylselanyl)-2-phenyl-propionaldehyde 
• 121034-40-0 2-Phenyl-2-phenylselanyl-propionaldehyde 
• 28478-27-5 4-(2-phenyl-propenyl)-morpholine 
• 75-09-2 dichloromethane 
• 98-86-2 acetophenone 

Downstream Products

• 81171-24-6 N-isopropyl-α-chloro-α-phenylaldimine 
• 25076-75-9 2-phenyl-2-piperidin-1-yl-propionaldehyde 
• 1418369-63-7 (RS)-5-phenyl-2,2,5-trimethyl-2,5-dihydro-1,3-thiazole 
• 161869-72-3 2-Chloro-2-phenyl-propionaldehyde O-methyl-oxime 
• 136846-88-3 rac-2-tert-Butyl-2,5-dihydro-5-methyl-5-phenyloxazol 
• 17325-55-2 (+/-)-2-chloro-2-phenyl-propionic acid 

Relevant articles and documents

Investigation of the Organocatalytic Chlorination of 2-Phenylpropanal

Results of an examination of the organocatalytic enantioselective α-chlorination of 2-phenylpropanal are described. Synthetic investigation including the screening of primary and secondary aminocatalysts, many different reaction conditions, and other α-br

The Rabe amination after a century: Direct addition of N-heterocycles to carbonyl compounds

A catalytic version of the Rabe electrophilic amination is presented. This kind of reaction was originally employed in 1918 in a key step for the conversion of quinotoxine to quinine. Ketones and α-substituted aldehydes give the corresponding α-aminated carbonyl compounds in moderate yield. α,α-Unsubstituted aldehydes give rise to amino ketones via a novel rearrangement.

Polymer-supported 4-(phenylseleno)morpholine as a useful α-selenenylating agent for saturated aldehydes. A highly efficient route to α-haloaldehydes on solid phase

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