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(+/-)-methyl cis-3-hydroxycyclohexanecarboxylate is an organic compound with the molecular formula C8H14O3, belonging to the class of cyclohexanecarboxylates. It is a mixture of two enantiomers, indicated by the "+/-" in its name, and exists as a white solid at room temperature with a molecular weight of 158.20 g/mol. (+/-)-methyl cis-3-hydroxycyclohexanecarboxylate has been studied for its potential pharmaceutical and medicinal applications, as well as its use in chemical synthesis and research.

6125-56-0

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6125-56-0 Usage

Uses

Used in Pharmaceutical and Medicinal Applications:
(+/-)-methyl cis-3-hydroxycyclohexanecarboxylate is used as a pharmaceutical and medicinal compound for its potential therapeutic properties. Its unique structure and properties make it a promising candidate for the development of new drugs and treatments.
Used in Chemical Synthesis and Research:
(+/-)-methyl cis-3-hydroxycyclohexanecarboxylate is also used as a chemical intermediate in the synthesis of various compounds. Its versatility and reactivity make it a valuable component in the development of new chemical processes and products. Additionally, it serves as a subject of research to further explore its properties and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 6125-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6125-56:
(6*6)+(5*1)+(4*2)+(3*5)+(2*5)+(1*6)=80
80 % 10 = 0
So 6125-56-0 is a valid CAS Registry Number.

6125-56-0Relevant academic research and scientific papers

1- (1-CYCLOHEXYL-4-PIPERIDINYL) -1, 3-DIHYDRO-2H-BENZIMIDAZOL-2-ONE DERIVATIVES WHICH HAVE ACTIVITY ON THE M1 RECEPTOR AND THEIR USE IN MEDICINE

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, (2008/12/04)

Compounds of formula (I) or a salt thereof are provided, wherein R4, R5, R6, Q and R are as defined in the description. Uses of the compounds as medicaments and in the manufacture of medicaments for treating psychotic disorders and cognitive impairments are disclosed. The invention further discloses pharmaceutical compositions comprising the compounds.

METHOD FOR THE PREPARATION OF ENANTIOMER FORMS OF CIS-CONFIGURED 3-HYDROXYCYCLOHEXANE CARBOXYLIC ACID DERIVATIVES USING HYDROLASES

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Page/Page column 18, (2008/06/13)

The present invention relates to a process for preparing chiral non-racemic cis-configured cyclohexanols or cyclohexanol derivatives of the formula (I) Cis-configured hydroxyl-cyclohexane carboxylic acid derivatives of formula (I) are central building blo

Enzymatic in vitro Reduction of Ketones. Part 13. Horse Liver Alcohol Dehydrogenase (HLAD) as a Tool for the Synthesis of Enantiomerically Pure Alkyl 3-oxo- and 3-hydroxycyclohexanecarboxylates.

Willaert, J. J.,Lemiere, G. L.,Dommisse, R. A.,Lepoivre, J. A.,Alderweireldt, F. C.

, p. 2401 - 2423 (2007/10/02)

Enantiomerically pure alkyl 3-oxocyclohexanecarboxylates and the corresponding alcohols have been prepared using HLAD as a suitable catalyst.Kinetic and thermodynamic parameters for the enzymatic reductions are given.The enantiomeric purity and the absolute configuration of the reaction products are determined.The alcohol moiety (methyl, isopropyl or pentyl) of the ester group influences both the steric course and the kinetics of the reduction.Side reactions of the substrate with the reaction medium can be avoided by an appropriate choice of the reaction conditions.

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