99065-34-6

Basic information

• Product Name: ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE
• Synonyms: Cyclopentanecarboxylic acid,1-(aminomethyl)-,ethyl ester;ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE
• CAS NO: 99065-34-6
• Molecular Formula: C₉H₁₇NO₂
• Molecular Weight: 171.24
• Mol File: 99065-34-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE(99065-34-6)
• EPA Substance Registry System: ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE(99065-34-6)

Safety Data

• Hazardous Substances Data: 99065-34-6(Hazardous Substances Data)

Usage

General Description

ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE is a chemical compound with the molecular formula C10H19NO2. It is a clear, colorless liquid with a faint odor and is commonly used as an intermediate in the manufacturing of pharmaceuticals and agrochemicals. ETHYL 1-(AMINOMETHYL)CYCLOPENTANECARBOXYLATE is known to have analgesic and anti-inflammatory properties and is used in the synthesis of various drugs. It is also used as a building block in organic chemistry reactions and is considered to be a versatile compound with potential applications in the pharmaceutical and agricultural industries.

Upstream product

• 28247-14-5 ethyl 1-cyanocyclopentanecarboxylate 
• 105-56-6 ethyl 2-cyanoacetate 
• 96042-30-7 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 

Downstream Products

• 204514-22-7 1-(<<(tert-butoxy)carbonyl>amino>methyl)cyclopentane-1-carboxylic acid 
• 137864-26-7 ethyl N-[(2'-cyanobiphenyl-4-yl)methyl]-1-aminomethylcyclopentane-1-carboxylate 

Relevant articles and documents

The design and synthesis of potent cyclic peptide VCAM-VLA-4 antagonists incorporating an achiral Asp-Pro mimetic

The Asp-Pro sequence of the cyclic peptide Ac-HN-Tyr-Cys*-Asp-Pro-Cys*-OH (1) could be replaced with the achiral dipeptide mimetic 1-(2-aminoethyl)cyclpentylcarboxylic acid with retention of potent inhibition of the VCAM-VLA-4 interaction. (C) Elsevier Science Ltd. All rights reserved.

ACYL COMPOUNDS

Compounds of the formula STR1 in which R 1 is an aliphatic hydrocarbon radical which is unsubstituted or substituted by halogen or hydroxyl, or a cycloaliphatic or araliphatic hydrocarbon radical; X 1 is CO, SO 2, or--O--C(=O)--with the carbon atom of the carbonyl group being attached to the nitrogen atom shown in formula I; X 2 is a divalent aliphatic hydrocarbon radical which is unsubstituted or substituted by hydroxyl, carboxyl, amino, guanidino or a cycloaliphatic or aromatic radical, or is a divalent cycloaliphatic hydrocarbon radical, it being possible for a carbon atom of the aliphatic hydrocarbon radical to be additionally bridged by a divalent aliphatic hydrocarbon radical; R. sub.2 is carboxyl which, if desired, is esterified or amidated, substituted or unsubstituted amino, formyl which, if desired, is acetalized, 1H-tetrazol-5-yl, pyridyl, hydroxyl which, if desired, is etherified, S(O) m--R where m is 0, 1 or 2 and R is hydrogen or an aliphatic hydrocarbon radical, alkanoyl, unsubstituted or N-substituted sulfamoyl or PO n H 2 where n is 2 or 3; X 3 is a divalent aliphatic hydrocarbon; R 3 is carboxyl, 5-tetrazolyl, SO. sub.3 H, PO. sub.2 H 2, PO 3 H 2 or haloalkylsulfamoyl; and the rings A and B independently of one another are substituted or unsubstituted; in free form or in salt form, can be prepared in a manner known per se and can be used, for example, as medicament active ingredients.