115730-35-3 Usage
Chemical structure
A cyclohexene ring with two carboxylic acid groups and an amino group at the 3-position.
Stereochemistry
Exists as a single enantiomer with the (S)configuration.
Reactivity
Unique chemical structure allows for various synthetic applications.
Applications
a. Synthesis of pharmaceuticals and organic compounds.
b. Building block for biologically active molecules.
c. Chiral auxiliary in asymmetric synthesis.
Potential interest
a. Biological activity for medicinal chemistry research.
b. Development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 115730-35-3 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 115730-35:
(8*1)+(7*1)+(6*5)+(5*7)+(4*3)+(3*0)+(2*3)+(1*5)=103
103 % 10 = 3
So 115730-35-3 is a valid CAS Registry Number.
115730-35-3Relevant academic research and scientific papers
Synthesis and resolution of DHCGA, a new conformationally rigid 3,4-dehydroglutamic acid analogue
Trigalo, Francois,Acher, Francine,Azerad, Robert
, p. 5203 - 5212 (2007/10/02)
(±)-1-amino-2-cyclohexene-1,3-dicarboxylic acid (DHCGA),an unsaturated cyclic analogue of glutamic acid, was prepared from 3-carboxy-4-cyclohexenone by a Bucherer-Bergs reaction. Resolution was performed through coupling with L-leucine and separation of the resulting diastereoisomeric dipeptides. Spectral data, including optical rotation and circular dichroism of both enantiomers of DHCGA are reported.
