187334-05-0 Usage
Uses
Used in Organic Synthesis:
[(1S,2R)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is used as a reagent or building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for versatile chemical reactions and the formation of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(1S,2R)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is used as a key intermediate in the development of new drugs. Its structural properties make it a valuable component in the synthesis of potential therapeutic agents.
Used in Agrochemicals:
[(1S,2R)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is also utilized in the agrochemical industry for the synthesis of novel compounds with pesticidal or herbicidal properties, contributing to the development of more effective and environmentally friendly products.
Used in Materials Science:
Within the field of materials science, [(1S,2R)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is explored for its potential applications in the development of new materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Overall, [(1S,2R)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is a compound of interest to researchers in the fields of chemistry, biochemistry, and pharmaceutical development due to its diverse potential applications and unique structural properties.
Check Digit Verification of cas no
The CAS Registry Mumber 187334-05-0 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 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 187334-05:
(8*1)+(7*8)+(6*7)+(5*3)+(4*3)+(3*4)+(2*0)+(1*5)=150
150 % 10 = 0
So 187334-05-0 is a valid CAS Registry Number.
187334-05-0Relevant 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.
Erhoehung der Effizienz der katalytischen asymmetrischen Aminohydroxylierung durch N-Halogencarbamat-Salze
Li, Guigen,Angert, Hubert H.,Sharpless, K. Barry
, p. 2995 - 2999 (2007/10/03)
Keywords: Aminoalkohole; Asymmetrische Aminohydroxylierung; Carbamate; Katalyse
