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57266-61-2

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  • 3-Cyclohexene-1-carboxylicacid, 6-amino-, ethyl ester, hydrochloride (1:1), (1R,6S)-rel-

    Cas No: 57266-61-2

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57266-61-2 Usage

Chemical Properties

light beige crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 57266-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,6 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57266-61:
(7*5)+(6*7)+(5*2)+(4*6)+(3*6)+(2*6)+(1*1)=142
142 % 10 = 2
So 57266-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-4,7-8H,2,5-6,10H2,1H3/p+1/t7-,8+/m1/s1

57266-61-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL CIS-2-AMINO-4-CYCLOHEXENE-1-CARBOXYLATE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names ethyl cis-2-aminocyclopentanecarboxylate hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57266-61-2 SDS

57266-61-2Relevant articles and documents

Alicyclic β- And γ-amino acids: Useful scaffolds for the stereocontrolled access to amino acid-based carbocyclic nucleoside analogs

Remete, Attila Márió,Kiss, Loránd

, (2019/01/21)

Stereocontrolled synthesis of some amino acid-based carbocyclic nucleoside analogs containing ring C=C bond has been performed on β- and γ-lactam basis. Key steps were N-arylation of readily available β- or γ-lactam-derived amino ester isomers and amino a

Stereoselective synthesis of hydroxylated β-aminocyclohexanecarboxylic acids

Kiss, Loránd,Forró, Eniko,Martinek, Tamás A.,Bernáth, Gábor,De Kimpe, Norbert,Fül?p, Ferenc

, p. 5036 - 5043 (2008/09/21)

A simple synthetic approach has been developed for the regio- and diastereoselective synthesis of hydroxylated 2-aminocyclohexanecarboxylic acid stereoisomers from 1,4-cyclohexadiene by the reductive opening of appropriate epoxide intermediates derived from the corresponding bicyclic β-lactams. This method has been extended to the synthesis of these hydroxylated β-amino acids in enantiomerically pure form.

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