Cas 772330-11-7,Cyclooctanecarboxylic acid, 2-amino-, ethyl ester, (1R,2S)- (9CI)

772330-11-7

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Basic information

Product Name: Cyclooctanecarboxylic acid, 2-amino-, ethyl ester, (1R,2S)- (9CI)
Synonyms: Cyclooctanecarboxylic acid, 2-amino-, ethyl ester, (1R,2S)- (9CI)
CAS NO:772330-11-7
Molecular Formula: C11H21NO2
Molecular Weight: 199.28994
EINECS: N/A
Product Categories: AMINOACID
Mol File: 772330-11-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 276.2±33.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 0.978±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 10.38±0.40(Predicted)
CAS DataBase Reference: Cyclooctanecarboxylic acid, 2-amino-, ethyl ester, (1R,2S)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclooctanecarboxylic acid, 2-amino-, ethyl ester, (1R,2S)- (9CI)(772330-11-7)
EPA Substance Registry System: Cyclooctanecarboxylic acid, 2-amino-, ethyl ester, (1R,2S)- (9CI)(772330-11-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 772330-11-7(Hazardous Substances Data)

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772330-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 772330-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,2,3,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 772330-11:
(8*7)+(7*7)+(6*2)+(5*3)+(4*3)+(3*0)+(2*1)+(1*1)=147
147 % 10 = 7
So 772330-11-7 is a valid CAS Registry Number.

772330-11-7Upstream product

772330-11-7Downstream Products

522644-10-6 (1R,2R)-2-aminocyclooctanecarboxylic acid hydrochloride

772330-11-7Relevant academic research and scientific papers

Synthesis of alicyclic trans-β-amino acids from cis-β- hydroxycycloalkane-carboxylates

Kiss, Lorand,Forro, Eniko,Bernath, Gabor,Fueloep, Ferenc

, p. 1265 - 1268 (2007/10/03)

A simple and efficient method is described for the preparation of both racemic and enantiopure trans-β-amino acids with a cycloheptane or cyclooctane skeleton, starting from racemic and enantiopure ethyl cis-2-hydroxycarboxylates. Georg Thieme Verlag Stut

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