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Dimethyl 2,3-diacetylsuccinate is a chemical compound with the molecular formula C8H12O6. It is a derivative of succinic acid and is commonly used as a building block in organic synthesis. This chemical is a diester formed by the condensation of two molecules of acetic anhydride with one molecule of succinic anhydride, and subsequent reaction with methanol. It is a white to off-white crystalline solid that is insoluble in water but soluble in organic solvents.

74536-45-1

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74536-45-1 Usage

Uses

Used in Pharmaceutical Industry:
Dimethyl 2,3-diacetylsuccinate is used as a synthetic intermediate for the production of pharmaceuticals due to its versatile reactivity and usefulness in organic synthesis.
Used in Agrochemical Industry:
Dimethyl 2,3-diacetylsuccinate is used as a building block in the synthesis of agrochemicals, contributing to the development of various agricultural products.
Used in Flavoring and Fragrance Industry:
Dimethyl 2,3-diacetylsuccinate is used as a flavoring agent and fragrant in the food and beverage industry, enhancing the taste and aroma of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 74536-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74536-45:
(7*7)+(6*4)+(5*5)+(4*3)+(3*6)+(2*4)+(1*5)=141
141 % 10 = 1
So 74536-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O6/c1-5(11)7(9(13)15-3)8(6(2)12)10(14)16-4/h7-8H,1-4H3

74536-45-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2,3-diacetylbutanedioate

1.2 Other means of identification

Product number -
Other names Butanedioicacid,2,3-diacetyl-,1,4-dimethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74536-45-1 SDS

74536-45-1Downstream Products

74536-45-1Relevant academic research and scientific papers

Chemical and Electrochemical Oxidative Dimerization of Carbonyl Compounds by Cerium(IV) Salts. A Comparative Study

Cho, Liu Yao,Romero, Jose Ricardo

, p. 8757 - 8760 (2007/10/02)

β-dicarbonyl and β-cyanocarbonyl compounds were dimerized chemically by CAN or by electrocatalysis using cerous nitrate as mediator.The saturated and unsaturated products of these oxidations are presented.

ELECTROCHEMICAL OXIDATIVE DIMERIZATION OF ACETOACETIC AND BENZOYLACETIC ESTERS IN THE PRESENCE OF METAL HALIDES

Elinson, M.N.,Lizunova, T.L.,Nikishin, G.I.

, p. 2213 - 2216 (2007/10/02)

Acetoacetic and benzoylacetic esters dimerize on electrolysis in the presence of metal halide mediators to form 2,5-dioxohexane-3,4-dicarboxylic and 1,4-dioxo-1,4-diphenylbutane-2,3-dicarboxylic esters in yields up to 90percent.Primarily the meso-form of the dimer is produced (up to 90percent) under optimal conditions (NaI, -20 deg C) in acetone and acetonitrile.Diastereomers of the dimer are produced in comparable amounts in methanol and ethanol.

Hypervalent Iodine Oxidation: α-Functionalization of β-Dicarbonyl Compounds Using Iodosobenzene

Moriarty, Robert, M.,Vaid, Radhe K.,Ravikumar, Vasulinga T.,Vaid, Beena K.,Hopkins, Thomas E.

, p. 1603 - 1608 (2007/10/02)

Hypervalent iodine oxidation of β-diketones and β-ketoesters with iodosobenzene-boron trifluoride etherate in chloroform using appropriate nucleophiles results in α-functionalization.Benzoylacetone on reaction with iodosobenzene or iodosobenzene boron trifluoride-etherate in methanol yields α-methoxyacetophenone (9) and methyl phenylacetate (10).The possible mechanisms for these reactions are discussed.

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