35392-80-4 Usage
Description
(2R,3S)-2,3-Diethylsuccinic acid, also known as succinic acid, is a dicarboxylic acid with a molecular formula of C8H14O4 and a molecular weight of 174.2 g/mol. It is a compound used in various industrial applications and is commonly used as a food additive, flavoring agent, and in the production of pharmaceuticals and polymers.
Uses
Used in Food Industry:
(2R,3S)-2,3-Diethylsuccinic acid is used as a food additive and flavoring agent for its ability to enhance the taste and quality of food products.
Used in Pharmaceutical Industry:
(2R,3S)-2,3-Diethylsuccinic acid is used as a building block in the synthesis of various pharmaceuticals due to its unique chemical properties.
Used in Polymer Industry:
(2R,3S)-2,3-Diethylsuccinic acid is used in the production of polymers, such as biodegradable plastics, due to its ability to form strong and stable polymer chains.
Used in Chemical Industry:
(2R,3S)-2,3-Diethylsuccinic acid is used in the manufacture of resins, lacquers, and dyes, where its chemical properties contribute to the desired characteristics of these products.
Production:
(2R,3S)-2,3-Diethylsuccinic acid is produced through the oxidation of n-butane or by fermentation of glucose.
Safety:
(2R,3S)-2,3-Diethylsuccinic acid is classified as a non-hazardous substance, making it safe for use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 35392-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,9 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35392-80:
(7*3)+(6*5)+(5*3)+(4*9)+(3*2)+(2*8)+(1*0)=124
124 % 10 = 4
So 35392-80-4 is a valid CAS Registry Number.
35392-80-4Relevant articles and documents
Reactions of Lithium Acylates α-Carbanions with 1,2-Diiodoethane
Zorin,Chanysheva,Lenkova,Zorin
, p. 148 - 150 (2019/04/08)
The interaction of lithium acylates α-carbanions (obtained via metallation of acetic, butyric, and isobutyric acids with lithium diisopropylamide) with 1,2-diiodoethane under argon in tetrahydrofuran at 20–25°C has proceeded as oxidative cross-coupling of enolate anions to form succinic, 2,3-diethylsuccinic, and 2,2,3,3-tetramethylsuccinic acids with yields 50, 53, and 16%, respectively. The products of sequential nucleophilic substitution of iodine atoms with alkyloxycarbonyl species have not been detected.
Reaction of α-carbanions of lithium acylates with 1,2-dibromoethane
Zorin,Zaynashev,Chanysheva,Zorin
, p. 1382 - 1385 (2015/08/03)
The reaction of 1,2-dibromoethane with α-carbanions of lithium acylates generated from acetic, butyric, isobutyric, and capronic acids with lithium diisopropylamide has been studied. Anion-radical and anionic pathways of the products formation have been discussed.
