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.
115730-36-4Relevant 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.