199679-86-2 Usage
Chemical Structure
C10H12ClNO2
Molecular Weight
213.67
Functional Groups
Amino acid, carboxylic acid, and phenyl ring
Physical State
White or off-white crystalline solid
Solubility
Slightly soluble in water, soluble in alcohol and acetone
Melting Point
211-214°C
Boiling Point
Not applicable as it is a solid
Mechanism of Action
Acts as a GABA-B receptor agonist, inhibiting the release of neurotransmitters in the central nervous system
Uses
Skeletal muscle relaxant and antispastic agent, commonly used to treat muscle spasticity in conditions such as multiple sclerosis and spinal cord injuries
Administration
Available in both oral and intrathecal forms, with the latter being administered directly into the spinal fluid for more targeted effects
Side Effects
Potential side effects may include drowsiness, dizziness, and fatigue.
Check Digit Verification of cas no
The CAS Registry Mumber 199679-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,7 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 199679-86:
(8*1)+(7*9)+(6*9)+(5*6)+(4*7)+(3*9)+(2*8)+(1*6)=232
232 % 10 = 2
So 199679-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClNO2/c1-2-9(10(13)14)12-8-5-3-7(11)4-6-8/h3-6,9,12H,2H2,1H3,(H,13,14)
199679-86-2Relevant academic research and scientific papers
Isosteres of chiral clofibric acid analogs: Synthesis, resolution, absolute configuration and HPLC detection of the optical purity
Ferorelli,Loiodice,Tortorella,Amoroso,Bettoni,Conte- Camerino,De Luca
, p. 367 - 374 (2007/10/03)
Both racemic and enantiomeric forms of some isosteres of chiral clofibric acid analogs have been synthesized. Also, the absolute configuration has been established by chemical correlation and the optical purity determined by a simple HPLC procedure. Moreover, these studies show that the isosteric substitution of the ether oxygen atom of α-aryloxy- alkanoic acids with sulfur, amino and methylene groups lead to compounds in which both biological activity and stereoselectivity regarding chloride channel are highly reduced.
