38052-23-2

Basic information

• Product Name: Cyclopentanecarboxylic acid, 2-amino-, ethyl ester
• Synonyms: Cyclopentanecarboxylic acid, 2-amino-, ethyl ester;ethyl 2-aMinocyclopentanecarboxylate
• CAS NO: 38052-23-2
• Molecular Formula: C₈H₁₅NO₂
• Molecular Weight: 157.21
• Mol File: 38052-23-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 213.4±33.0 °C(Predicted)
• Appearance: /
• Density: 1.045±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 10.10±0.40(Predicted)
• CAS DataBase Reference: Cyclopentanecarboxylic acid, 2-amino-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopentanecarboxylic acid, 2-amino-, ethyl ester(38052-23-2)
• EPA Substance Registry System: Cyclopentanecarboxylic acid, 2-amino-, ethyl ester(38052-23-2)

Safety Data

• Hazardous Substances Data: 38052-23-2(Hazardous Substances Data)

Upstream product

• 22031-52-3 2-aza-3-oxobicyclo<3.2.0>heptane 
• 64-17-5 ethanol 
• 1033755-97-3 2-benzylamino-cyclopentanecarboxylic acid ethyl ester 
• 7149-18-0 ethyl 2-amino-1-cyclopentene-1-carboxylate 
• 611-10-9 2-ethoxycarbonyl-1-cyclopentanone 
• 142-29-0 cyclopentene 
• 22031-52-3 cis-2-aza-3-oxobicyclo<3.2.0>heptane 

Downstream Products

• 197916-36-2 ethyl (1R,2S)-2-aminocyclopentane-1-carboxylate 
• 135053-11-1 cis-2-amino-1-cyclopentanecarboxamide 
• 135053-11-1 trans-2-aminocyclopentanecarboxamide 
• 128668-89-3 cis-3-phenyl-1,2,3,4a,5,6,7,7a-octahydrocyclopentapyrimidine-2,4-dione 
• 158262-07-8 ethyl cis-2-benzylamino-1-cyclopentanecarboxylate 
• 141045-77-4 Ethyl trans-2-(N-Benzylamino)cyclopentanecarboxylate 

Relevant articles and documents

SUBSTITUTED PYRROLO-PYRIDINONE DERIVATIVES AND THERAPEUTIC USES THEREOF

Compounds of formula (I), processes for their production and their use as pharmaceuticals.

Dirhodium(II)-Catalyzed (3 + 2) Cycloaddition of the N-Arylaminocyclopropane with Alkene Derivatives

Several (3 + 2) cycloaddition reactions catalyzed by dirhodium(II) complexes between N-arylaminocyclopropane and alkenes derivative have been developed. Preliminary mechanism studies suggest that dirhodium(II) complexes may decrease the bond-dissociation

Expanding dynamic kinetic protocols: Transaminase-catalyzed synthesis of α-substituted β-amino ester derivatives

Several α-alkylated β-amino esters have been obtained via DKR processes employing a kit of transaminases and isopropylamine as an amino donor in aqueous medium under mild conditions. Thus, while acyclic α-alkyl-β-keto esters afforded excellent conversions and enantioselectivities, although usually low diastereoselectivities, using more constrained cyclic β-keto esters high to excellent inductions were obtained.