41088-52-2 Usage
Description
3,4-Epoxycyclohexane carboxylic acid, methyl ester is an organic compound that serves as a valuable reagent in the field of organic synthesis. It is characterized by its colorless transparent liquid appearance, which indicates its potential for use in various chemical reactions without imparting color to the final product.
Uses
Used in Organic Synthesis:
3,4-Epoxycyclohexane carboxylic acid, methyl ester is used as a reagent for organic synthesis due to its unique chemical structure and properties. Its epoxy and ester functional groups make it a versatile building block for the creation of a wide range of compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,4-Epoxycyclohexane carboxylic acid, methyl ester is used as an intermediate for the synthesis of various drugs. Its ability to participate in a variety of chemical reactions, such as ring-opening reactions and esterification, allows for the development of complex molecular structures with potential therapeutic applications.
Used in Agrochemical Industry:
3,4-Epoxycyclohexane carboxylic acid, methyl ester is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its chemical properties make it suitable for the development of compounds that can effectively target and control pests, thereby contributing to increased crop yields and improved agricultural productivity.
Used in Specialty Chemicals:
In the specialty chemicals sector, 3,4-Epoxycyclohexane carboxylic acid, methyl ester is employed as a key component in the production of various high-value chemicals. Its unique properties enable the creation of specialty products with specific applications, such as additives for the plastics and coatings industries, or as components in the formulation of advanced materials with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 41088-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41088-52:
(7*4)+(6*1)+(5*0)+(4*8)+(3*8)+(2*5)+(1*2)=102
102 % 10 = 2
So 41088-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O3/c1-10-8(9)5-2-3-6-7(4-5)11-6/h5-7H,2-4H2,1H3
41088-52-2Relevant articles and documents
Preparation method of edoxaban intermediate
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, (2018/04/03)
The invention discloses a preparation method of edoxaban intermediate (1S, 3R, 4R)-3-tert-butoxycarbonylamino-4-hydroxy-cyclohexanecarboxylic acid. According to the preparation method, 3-amino-4-hydroxy-cyclohexane carboxylate represented by formula IV is taken as a raw material, protective reaction with amino protection groups is carried out so as to obtain 3-tert-butoxycarbonylamino-4-hydroxy-cyclohexane carboxylate represented by formula V, enzyme catalyzed esterification resolution reaction is carried out so as to obtain optically pure (1S, 3R, 4R)-3-tert-butoxycarbonylamino-4-hydroxy-cyclohexane carboxylate represented by formula VII, and at last lithium hydroxide hydrolysis is adopted so as to obtain the (1S, 3R, 4R)-3-tert-butoxycarbonylamino-4-hydroxy-cyclohexanecarboxylic acid represented by formula VI. The preparation method possesses following advantages: operation is simple, the preparation method is green, is friendly to the environment, and is high in selectivity and lowin cost, large scale industrialized production can be realized, and it is convenient for industrial popularization.
General Syntheses of 6- and 7-Carbomethoxy-trans-1-heteradecalins and 6- and 7-Carbomethoxy-trans-2-heteradecalins
Hirsch, Jerry A.,Truc, Vu Chi
, p. 2218 - 2227 (2007/10/02)
Two routes to all of the title compounds in the oxa and aza series have been studied.The most general path, involving a cyclohexene oxide intermediate, was not successful becauase of difficulty in separating regioisomers.Allylation of 4-carbomethoxycyclohexanone (11) followed by reduction produced the required trans-disubstituted allyl alcohols, which were converted to all of the desired 6-carbomethoxy-trans-1-heteradecalins.The allyl ketones were subjected to a homologation-side chain contraction sequence to produce the 6-carbomethoxy-trans-2-heteradecalins.Allylation of 3-carbomethoxycyclohexanone (12) was not regioselective, but all four product isomers were characterized.The desired 5-carbomethoxy-2-allylcyclohexanone isomers (27 and 28) were converted to the 7-carbomethoxy-trans-decalins by similar series of reactions
