10359-15-6 Usage
Description
2-Cyano-succinic acid diethyl ester is a chemical compound that belongs to the ester class, resulting from the reaction between an alcohol and an acid. It features a cyano group (CN), a functional group composed of a carbon atom triple-bonded to a nitrogen atom. 2-CYANO-SUCCINIC ACID DIETHYL ESTER may be utilized in various chemical synthesis processes due to its molecular structure and reactivity. However, its specific properties, toxicity, and other data require further investigation to provide accurate information. It is crucial to handle this compound with caution due to potential health risks associated with exposure.
Uses
Used in Chemical Synthesis:
2-Cyano-succinic acid diethyl ester is used as a chemical intermediate for various synthesis processes due to its molecular structure and reactivity. Its cyano group and ester linkage provide unique properties that can be exploited in the creation of different compounds.
Used in Pharmaceutical Industry:
2-Cyano-succinic acid diethyl ester is used as a building block in the synthesis of pharmaceutical compounds. Its reactivity and functional groups can be utilized to create new drug molecules with potential therapeutic applications.
Used in Material Science:
2-Cyano-succinic acid diethyl ester is used as a precursor in the development of new materials with specific properties. Its chemical structure can be incorporated into polymers, coatings, or other materials to achieve desired characteristics, such as improved strength, flexibility, or chemical resistance.
Used in Research and Development:
2-Cyano-succinic acid diethyl ester is used as a research compound in academic and industrial laboratories. Its unique properties and reactivity make it a valuable tool for studying chemical reactions, mechanisms, and the development of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 10359-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10359-15:
(7*1)+(6*0)+(5*3)+(4*5)+(3*9)+(2*1)+(1*5)=76
76 % 10 = 6
So 10359-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO4/c1-3-13-8(11)5-7(6-10)9(12)14-4-2/h7H,3-5H2,1-2H3
10359-15-6Relevant articles and documents
-
Raha
, p. 4098 (1953)
-
SYNTHESIS OF CYANOCARBOXYLIC ACID ALKYL ESTERS
-
Page/Page column 30-31, (2013/08/28)
Provided is a process for obtaining a compound of formula (I): N≡C-CH2-A-C(O)-OR, wherein Hal is halogen selected from F, Cl, Br or I, A denotes a bond or a divalent spacer selected from alkylene and arylene groups, and R is a C1-4 alkyl group, by reacting a compound of formula (II): Hal-CH2-A-C(O)-OR, wherein Hal is a halogen atom selected from F, Cl, Br and I, and wherein A and R are as defined above, with hydrogen cyanide in the presence of a first base, wherein the molar ratio between hydrogen cyanide and said first base is from 1:0.3 to 1:0.95 and the molar ratio between hydrogen cyanide to the compound of formula (II) is at least 1:1.
Process for production of 2,5 dioxopyrrolidine 3 carboxylate
-
Page/Page column 6, (2011/08/08)
The present invention provides a novel intermediate which enable to prepare tetrahydropyrrolo[1,2-a]pyrazin-4-spiro-3′-pyrrolidine derivatives such as Ranirestat being promising therapeutic agents for diabetic complications in a short process and in an economically advantageous and safe manner, and a process for preparing the same. That is, the present invention provides a process for preparing a compound of the following formula (I) wherein R1 is an amino group protected with a protecting group, etc., and R2 is a lower alkyl group, etc., comprising the following steps (1) and (2): (1) a step of converting a cyano group in a compound of the following formula (II) wherein n and m are each independently 0 or 1; provided when n is 0 and m is 1, then R2 and R3 are the same or different protecting groups for a carboxyl group; and when n is 1 and m is 0, then R2 and R3 are the same protecting groups for a carboxyl group; and R1 is as defined above, into a carbamoyl group in the presence of divalent palladium compound(s), primary amide(s) and water; and (2) a step of cyclizing the product obtained in the step (1).