30358-61-3 Usage
Description
(S)-(+)-2-amino-2-cyclohexylpropionic acid, also known as 2-amino-2-cyclohexylpropionic acid or l-homotaurine, is a chiral amino acid derivative that features a cyclohexane ring, an amino group, and a carboxylic acid group. It has been studied for its potential neuroprotective and antioxidant properties, which are believed to play a role in regulating neurotransmitter levels and protecting against oxidative damage in the brain.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-2-amino-2-cyclohexylpropionic acid is used as a precursor for the synthesis of various pharmaceuticals due to its unique chemical structure and potential therapeutic properties.
Used in Neurodegenerative Disease Treatment:
(S)-(+)-2-amino-2-cyclohexylpropionic acid is used as a therapeutic agent for treating neurodegenerative diseases and cognitive impairments, leveraging its potential neuroprotective and antioxidant properties to help regulate neurotransmitter levels and protect the brain from oxidative damage.
Used in Cognitive Impairment Treatment:
(S)-(+)-2-amino-2-cyclohexylpropionic acid is also used as a therapeutic agent for cognitive impairments, potentially enhancing cognitive function and providing neuroprotection through its antioxidant and neurotransmitter-regulating effects.
Check Digit Verification of cas no
The CAS Registry Mumber 30358-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30358-61:
(7*3)+(6*0)+(5*3)+(4*5)+(3*8)+(2*6)+(1*1)=93
93 % 10 = 3
So 30358-61-3 is a valid CAS Registry Number.
30358-61-3Relevant articles and documents
Applications of the sulfinimine-mediated asymmetric strecker synthesis to the synthesis of α-alkyl α-amino acids
Davis,Lee,Zhang,Fanelli
, p. 8704 - 8708 (2007/10/03)
Addition of Et2AlCN and i-PrOH to ketosulfinimines (N-sulfinyl imines) affords corresponding α-alkyl α-amino nitriles in moderate to good yields. The diastereoselectivity is largely dependent on the E/Z isomer ratio of the ketosulfinimine. Hydrolysis of the diastereomerically pure amino nitriles affords enantiopure α-alkyl α-amino acids in moderate to good yields.
