69164-36-9 Usage
Type of compound
Cyclic amino acid
Structure
Contains a cyclohexane ring with an ethyl group attached to the fourth carbon and an amino and carboxylic acid group attached to the first carbon
Industry use
Commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceuticals and bioactive compounds
Therapeutic applications
Studied for its potential as an anti-inflammatory and analgesic agent
Research value
Unique structure makes it a valuable tool for studying the structure-activity relationships of cyclic amino acids and their biological properties
Check Digit Verification of cas no
The CAS Registry Mumber 69164-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69164-36:
(7*6)+(6*9)+(5*1)+(4*6)+(3*4)+(2*3)+(1*6)=149
149 % 10 = 9
So 69164-36-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2/c1-2-7-3-5-9(10,6-4-7)8(11)12/h7H,2-6,10H2,1H3,(H,11,12)
69164-36-9Relevant academic research and scientific papers
Synthesis and tumorinhibiting activity of lanthanum(III) complexes with some 1-aminocycloalkancarboxylic acids
Kovachev,Ivanov,Buyukliev,Konstantinov,Karaivanova
, p. 25 - 27 (2007/10/02)
Complexes of La(III) with 1-aminocyclopentane-, -hexane, -heptane and -4-ethylcyclohexanecarboxylic acids were obtained. The compounds were characterized by elemental analyses, IR spectroscopy and conductivity measurements. The following general formula was derived: LaL3Cl3·5 H2O, where L is the corresponding 1-aminocycloalkanecarboxylic acid. The pharmacological studies showed that all complexes manifested higher cytostatic and cytotoxic effects in comparison with lanthanum chloride. Much higher cytotoxic (anti-P388/D1) and cytostatic (anti-L-1210 and antimelanoma-B16) activity was found for the lanthanum complex with 1-aminocyclopentanecarboxylic acid.
