187333-96-6 Usage
Description
[(1R,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is a carbamic acid derivative featuring a phenylmethyl ester group and a cyclohexyl carbanion intermediate. [(1R,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is characterized by its unique stereochemistry and structural composition, which may contribute to its potential applications in various fields, particularly in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
[(1R,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is used as a potential drug candidate for the treatment of various medical conditions due to its unique chemical structure and properties. Further investigation and testing are required to explore its specific applications and therapeutic potential.
Used in Drug Development:
In the field of drug development, [(1R,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester may serve as a starting point for the synthesis of novel compounds with improved pharmacological properties. Its unique stereochemistry and structural features could be exploited to design new drugs with enhanced efficacy and selectivity.
Used in Chemical Research:
As a carbamic acid derivative with a phenylmethyl ester group, [(1R,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester can be utilized in chemical research to study the reactivity and functional group interactions of carbamic acid derivatives. This may lead to a better understanding of their chemical behavior and potential applications in various industries.
Used in Material Science:
The unique structural features of [(1R,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 187333-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,3,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 187333-96:
(8*1)+(7*8)+(6*7)+(5*3)+(4*3)+(3*3)+(2*9)+(1*6)=166
166 % 10 = 6
So 187333-96-6 is a valid CAS Registry Number.
187333-96-6Relevant articles and documents
NICOTINAMIDE DERIVATIVES USEFUL AS PDE4 INHIBITORS
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Page/Page column 85-86, (2010/02/10)
This invention relates to nicotinamide derivatives of formula (I) and to pharmaceutical compositions containing, and the uses of such derivatives as PDE4 inhibitors wherein R7 is attached to the 3-or 4-position of the phenyl ring and is S(O)pR8, R8 is (C1-C4)alkyl optionally substituted by (C3-C6)cycloalkyl; m is 0 or 1; L is a (C3-C8)carbocyclic non-aromatic ring; and the remaining variables are as defined in the claims.
Kinetic resolution of amino alcohol derivatives with a chiral nucleophilic catalyst: Access to enantiopure cyclic cis-amino alcohols
Kawabata,Yamamoto,Momose,Yoshida,Nagaoka,Fuji
, p. 2700 - 2701 (2007/10/03)
Acylative kinetic resolution of racemic cyclic cis-amino alcohol derivatives with a chiral nucleophilic catalyst proceeds enantioselectively (s = 10-21) at ambient temperature to give enantiopure recovered materials, and the % conversion of the acylation can be readily controlled by the amount of acid anhydride.
Enzymatic resolution of (±)-cis-2-aminocyclopentanol and (±)-cis-2- aminocyclohexanol
Luna, Amparo,Astorga, Covadonga,Fueloep, Ferenc,Gotor, Vicente
, p. 4483 - 4487 (2007/10/03)
(±)-cis-N-Benzyloxycarbonyl-2-aminocyclopentanol was efficiently resolved by O-acylation with Pseudomonas cepacia lipase, as was (±)-cis-N- benzyloxycarbonyl-2-aminocyclohexanol when Candida antarctica lipase was used.
