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25306-99-4

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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

25306-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-(methoxymethyl)butanedioate

1.2 Other means of identification

Product number -
Other names Dimethyl (methoxymethyl)succinate

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:25306-99-4 SDS

25306-99-4Downstream Products

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.

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