63141-02-6

Basic information

• Product Name: Cyclopropanecarboxylic acid, 1-amino-2-(4-chlorophenyl)-, hydrochloride
• CAS NO: 63141-02-6
• Molecular Formula: C10H10ClNO2.ClH
• Molecular Weight: 248.109
• Mol File: 63141-02-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclopropanecarboxylic acid, 1-amino-2-(4-chlorophenyl)-, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-amino-2-(4-chlorophenyl)-, hydrochloride(63141-02-6)
• EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-amino-2-(4-chlorophenyl)-, hydrochloride(63141-02-6)

Safety Data

• Hazardous Substances Data: 63141-02-6(Hazardous Substances Data)

Upstream product

• 39645-27-7 (1S,3S)-1-(4-Chloro-phenyl)-5-phenyl-6-oxa-4-aza-spiro[2.4]hept-4-en-7-one 
• 15601-44-2 (Z)-2-phenyl-4-(4-chlorobenzylidene)-5(4H)-oxazolone 
• 97364-80-2 (1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester 
• 74444-84-1 Potassium; 2-(4-chloro-phenyl)-1-ethoxycarbonyl-cyclopropanecarboxylate 
• 74444-85-2 1-Azidocarbonyl-2-(4-chloro-phenyl)-cyclopropanecarboxylic acid 
• 74444-83-0 2-(4-chlorophenyl)cyclopropane-1,1-dicarboxylic acid diethyl ester 
• 6827-40-3 diethyl 4-chlorobenzylidenemalonate 
• 97364-31-3 (1S,2S)-2-(4-Chloro-phenyl)-1-isocyanato-cyclopropanecarboxylic acid methyl ester 
• 39645-04-0 (1R,2R)-1-Benzoylamino-2-(4-chloro-phenyl)-cyclopropanecarboxylic acid methyl ester 
• 39645-27-7 (1R,3S)-1-(4-Chloro-phenyl)-5-phenyl-6-oxa-4-aza-spiro[2.4]hept-4-en-7-one 
• 57427-86-8 (4E)-4-(4-chlorobenzylidene)-2-phenyloxazol-5(4H)-one 
• 97381-36-7 1-(4-Chloro-phenyl)-6,6-dimethyl-5,7-dioxa-spiro[2.5]octane-4,8-dione 
• 97364-50-6 (1R,2R)-1-Carbamoyl-2-(4-chloro-phenyl)-cyclopropanecarboxylic acid 
• 97364-58-4 (1S,2R)-2-(4-Chloro-phenyl)-1-methoxycarbonylamino-cyclopropanecarboxylic acid 

Downstream Products

• 74444-91-0 (1S,2S)-1-(2-Chloro-acetylamino)-2-(4-chloro-phenyl)-cyclopropanecarboxylic acid 

Relevant articles and documents

Expanding the scope of donor/acceptor carbenes to N -phthalimido donor groups: Diastereoselective synthesis of 1-cyclopropane α-amino acids

Warming of 4-phthalimido-N-mesyl-1,2,3-triazole in the presence of alkenes followed by silica gel induced hydrolysis results in a highly diastereoselective and catalyst-free entry to N-phthalimidocyclopropanecarboxaldehydes.

Synthesis of (E)- and (Z)-1-Amino-2-aryl(methyl)-cyclopropanecarboxylic Acids via Spirooxazolones

-