74536-45-1 Usage
Description
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.
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
74536-45-1Relevant articles and documents
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.
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.
