(R)-Carisbamate

Base Information

• Chemical Name: (R)-Carisbamate
• CAS No.: 194085-74-0
• Molecular Formula: C₉H₁₀ClNO₃
• Molecular Weight: 215.636
• UNII: QZ244ZS2F7
• Wikidata: Q5039678
• ChEMBL ID: CHEMBL4779038
• Mol file: 194085-74-0.mol

Synonyms:(R)-Carisbamate;194085-74-0;QZ244ZS2F7;1,2-Ethanediol, 1-(2-chlorophenyl)-, 2-carbamate, (1R)-;(R)-2-(2-Chlorophenyl)-2-hydroxyethyl carbamate;194085-74-0 (R-isomer);RWJ-452399;(2R)-2-(2-chlorophenyl)ethyl carbamate;(R)-2-carbamoyloxy-1-o-chlorophenylethanol;(1R)-1-(2-Chlorophenyl)-1,2-ethanediol 2-Carbamate;1,2-Ethanediol, 1-(2-chlorophenyl)-, 2-carbamate, (R)-;[(2R)-2-(2-chlorophenyl)-2-hydroxyethyl] carbamate;UNII-QZ244ZS2F7;SCHEMBL1037665;CHEMBL4779038;OLBWFRRUHYQABZ-QMMMGPOBSA-N;EX-A3231;AKOS027446305;FT-0664382;E87481;(R)-2-(2-Chlorophenyl)-2-hydroxyethylcarbamate;Q5039678;carbamic acid (2R)-2-(2-chloro-phenyl)-2-hydroxy-ethyl ester

Chemical Property of (R)-Carisbamate

Chemical Property:

• Melting Point: 131-133°C
• PSA: 73.54000
• LogP: 1.98250
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: Chloroform (Slightly, Sonicated), DMSO (Slightly)
• XLogP3: 1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 215.0349209
• Heavy Atom Count: 14
• Complexity: 201

Purity/Quality:

99.90% ^*data from raw suppliers

(R)-Carisbamate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C(COC(=O)N)O)Cl
• Isomeric SMILES: C1=CC=C(C(=C1)[C@H](COC(=O)N)O)Cl
• Uses: Carisbamate is being developed for adjuvant treatment of partial onset epilepsy. Carisbamate produces anticonvulsant effects in primary generalized, complex partial and absence-type seizure models, and exhibits neuroprotective and antiepileptogenic properties in rodent epilepsy models. Carisbamate is being developed for adjuvant treatment of partial onset epilepsy. Carisbamate produces anticonvulsant effects in primary generalized, complex partial and absence-type seizure models, and exhibits neuroprotective and antiepileptogenic properties in rodent epilepsy models. Neuroprotective & Neuroresearch Product. Acts as a novel neuromodulator with a little evidence of CYP metabolism.