105307-53-7 Usage
Uses
Used in Pharmaceutical Industry:
(R)-ENDO-CIS-2-AZABICYCLO[3.3.0]OCTANE-3-CARBOXYLIC ACID is used as a muscle relaxant for the treatment of muscle spasticity. Its agonistic effect on GABAB receptors helps to alleviate the symptoms by reducing the hyperactivity of motor neurons, providing relief to patients suffering from conditions like multiple sclerosis or spinal cord injuries.
Used in Neurological Treatments:
(R)-ENDO-CIS-2-AZABICYCLO[3.3.0]OCTANE-3-CARBOXYLIC ACID is utilized as a therapeutic agent in the management of neurological disorders characterized by increased muscle tone. Its ability to modulate neurotransmitter activity makes it a valuable asset in the treatment of such conditions.
Used in Psychiatric Treatments:
(R)-ENDO-CIS-2-AZABICYCLO[3.3,0]OCTANE-3-CARBOXYLIC ACID is being explored for its potential use in treating alcohol dependence and withdrawal symptoms. Its impact on neurotransmitter levels suggests that it may help in reducing cravings and managing the severity of withdrawal symptoms, offering a new approach to addiction treatment.
Used in Research and Development:
(R)-ENDO-CIS-2-AZABICYCLO[3.3.0]OCTANE-3-CARBOXYLIC ACID is employed in scientific research to further understand the role of GABAB receptors in various physiological and pathological processes. Its use in experimental models aids in the development of new therapeutic strategies for a range of neurological and psychiatric conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 105307-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,0 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105307-53:
(8*1)+(7*0)+(6*5)+(5*3)+(4*0)+(3*7)+(2*5)+(1*3)=87
87 % 10 = 7
So 105307-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c10-8(11)7-4-5-2-1-3-6(5)9-7/h5-7,9H,1-4H2,(H,10,11)/t5?,6-,7?/m1/s1
105307-53-7Relevant academic research and scientific papers
COUPLING OF β-ACETAMIDO RADICALS WITH α-CHLORO ACRYLONITRILE - A NEW ACCESS TO DISUBSTITUTED PROLINE DERIVATIVES
Henning, R.,Urbach, H.
, p. 5343 - 5346 (2007/10/02)
β-Acetamido radicals are prepared by reduction of organomercurials and coupled with α-chloro-acrylonitrile.The coupling products are further converted to proline derivatives.