181289-25-8 Usage
Description
(3S)-3-(2-methoxy-2-oxoethyl)-5-methylhexanoic acid is an organic compound with a unique molecular structure that features a 3S stereochemistry, a 2-methoxy-2-oxoethyl group, and a 5-methylhexanoic acid backbone. (3S)-3-(2-methoxy-2-oxoethyl)-5-methylhexanoic acid has potential applications in various industries due to its specific chemical properties and reactivity.
Uses
Used in Pharmaceutical Industry:
(3S)-3-(2-methoxy-2-oxoethyl)-5-methylhexanoic acid is used as an impurity in the synthesis of Pregabalin (P704800), a GABA analogue that serves as an anticonvulsant. The presence of this compound as an impurity in Pregabalin production is significant, as it can impact the quality and efficacy of the final pharmaceutical product.
Used in Chemical Research:
(3S)-3-(2-methoxy-2-oxoethyl)-5-methylhexanoic acid can be utilized as a starting material or intermediate in the synthesis of various complex organic molecules, particularly those with chiral centers or specific functional groups. Its unique structure makes it a valuable compound for research and development in the field of organic chemistry.
Used in Material Science:
The compound's specific molecular structure may also find applications in the development of new materials with tailored properties, such as polymers with specific mechanical, thermal, or chemical characteristics. Further research and development in this area could lead to innovative materials with a wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 181289-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,8 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 181289-25:
(8*1)+(7*8)+(6*1)+(5*2)+(4*8)+(3*9)+(2*2)+(1*5)=148
148 % 10 = 8
So 181289-25-8 is a valid CAS Registry Number.
181289-25-8Relevant articles and documents
Preparation method and application of high-purity dimethyl 3-isobutylglutarate
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, (2019/12/02)
The invention provides a preparation method and application of high-purity dimethyl 3-isobutylglutarate. Specifically, the invention provides the method for preparing dimethyl 3-isobutylglutarate shown as a formula 2, and the method comprises the step of enabling 3-isobutylglutaric acid to react in methanol in the presence of potassium permanganate and concentrated sulfuric acid, so as to obtain the high-purity dimethyl 3-isobutylglutarate. The method is simple, easy to control, high in product conversion rate, mild in reaction condition, convenient for industrial production and low in cost, the product is easy to purify, and the purity is up to 99% or above.
CAL-B catalyzed desymmetrization of 3-alkylglutarate: "olefin effect" and asymmetric synthesis of pregabalin
Jung, Jae-Hoon,Yoon, Doo-Ha,Kang, Philjun,Lee, Won Koo,Eum, Heesung,Ha, Hyun-Joon
, p. 3635 - 3641 (2013/06/26)
CAL-B catalyzed desymmetrization of prochiral 3-alkylglutaric acid diesters was performed to prepare optically active 3-alkylglutaric acid monoesters bearing various alkyl substituents, including methyl, ethyl, propyl and allyl groups. Allyl esters showed
A process for the preparation of a (S)(+)-3-(aminomethyl)-5-methylhexanoic acid
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Page/Page column 9, (2008/12/09)
A process for the preparation of (S)(+)-3-(aminomethyl)-5-methylhexanoic acid (pregabalin) of formula (I) or a salt thereof, comprising the reaction of a compound of formula (II) with an alcohol ROH, in the presence or absence of enzyme, to give a compound of formula (III) as herein defined the transformation of a compound of formula (III) into a compound of formula (VI) or (VIII) as herein defined, and the subsequent hydrolysis of a compound of formula (VI) or (VIII), to give pregabalin.
