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115730-36-4

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115730-36-4 Usage

General Description

1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI) is a chemical compound with the molecular formula C8H13NO4. It is a derivative of cyclohexane and contains both carboxylic acid and amino functional groups. 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI) has potential applications in pharmaceuticals, polymers, and other industrial processes. It may have properties that make it useful as a building block for the synthesis of various organic molecules. Its stereochemistry, with one of the carboxylic acid groups in a trans configuration, may also impart specific reactivity or selectivity in certain chemical reactions. Further research and development may uncover additional uses and potential benefits of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 115730-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115730-36:
(8*1)+(7*1)+(6*5)+(5*7)+(4*3)+(3*0)+(2*3)+(1*6)=104
104 % 10 = 4
So 115730-36-4 is a valid CAS Registry Number.

115730-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)

1.2 Other means of identification

Product number -
Other names -

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

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

More Details:115730-36-4 SDS

115730-36-4Relevant articles and documents

Resolution and regioselective protection of glutamic acid analogues. I- Resolution of diastereomeric α-boroxazolidone derivatives

Acher,Azerad

, p. 731 - 744 (2007/10/02)

Diastereomeric α-boroxazolidone γ-phenylethylamide (or γ-phenylethanolamide) derivatives of 2-, 3- or 4-substituted glutamic acid analogues have been separated by silicagel chromatography, resulting, after deprotection, in a practical method for the resolution of most of these unnatural amino acids.

CHEMOENZYMATIC SYNTHESIS OF CONFORMATIONALLY RIGID GLUTAMIC ACID ANALOGUES

Trigalo, F.,Buisson, D.,Azerad, R.

, p. 6109 - 6112 (2007/10/02)

All stereomers of cyclohexane cyclopentane-derived analogues of glutamic acid have been synthesized from the corresponding 3-keto-cycloalkyl carboxylic acid esters by a combination of microbial steps and standard chemical methods.

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