25306-99-4 Usage
General Description
Dimethyl (methoxymethyl)succinate is a chemical compound that is used in various industrial applications. It is a colorless liquid with a fruity odor and is commonly used as a solvent, intermediate, or starting material in the production of specialty chemicals and pharmaceuticals. Its chemical structure consists of two methyl groups, a methoxy group, and a succinate ester group, which gives it its unique properties and reactivity. Dimethyl (methoxymethyl)succinate is known for its high stability and low toxicity, making it a versatile and valuable ingredient in the manufacturing of a wide range of products. Additionally, it is considered relatively safe for use and handling in controlled settings.
Check Digit Verification of cas no
The CAS Registry Mumber 25306-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,0 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25306-99:
(7*2)+(6*5)+(5*3)+(4*0)+(3*6)+(2*9)+(1*9)=104
104 % 10 = 4
So 25306-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O5/c1-11-5-6(8(10)13-3)4-7(9)12-2/h6H,4-5H2,1-3H3
25306-99-4Relevant articles and documents
Organocatalytic head-to-tail dimerization of methacrolein via conjugate addition of methanol: An alcohol activation mechanism proved by electrospray ionization mass spectrometry
Matsuoka, Shin-Ichi,Shimakawa, Shintaro,Takagi, Koji,Suzuki, Masato
supporting information; experimental part, p. 6835 - 6838 (2012/01/03)
The head-to-tail dimerization of methacrolein via the conjugate addition of methanol is catalyzed by various organic bases, such as an amine, phosphine, and N-heterocyclic carbene, to give 2,4-dimethyl-2-methoxymethylpentane-1,5-dial in moderate yields. Based on the interpretation of the key intermediates by electrospray ionization mass spectrometry, we propose a reaction mechanism involving the initial conjugate addition of the organic bases to methacrolein to generate a zwitterionic base followed by the activation of methanol.