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24889-15-4

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24889-15-4 Usage

General Description

ACETONYLMALONIC ACID DIMETHYL ESTER is a chemical compound with the molecular formula C9H14O4. It is a colorless liquid with a fruity odor, commonly used as a reagent in organic synthesis. ACETONYLMALONIC ACID DIMETHYL ESTER is often utilized in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as an intermediate in the synthesis of various active ingredients in the pharmaceutical and agrochemical industries. Additionally, it is used as a solvent in some organic reactions. However, it is important to handle ACETONYLMALONIC ACID DIMETHYL ESTER with caution as it is flammable and may cause irritation upon contact with skin or eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 24889-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,8 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24889-15:
(7*2)+(6*4)+(5*8)+(4*8)+(3*9)+(2*1)+(1*5)=144
144 % 10 = 4
So 24889-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O5/c1-5(9)4-6(7(10)12-2)8(11)13-3/h6H,4H2,1-3H3

24889-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-(2-oxopropyl)propanedioate

1.2 Other means of identification

Product number -
Other names acetony,malonate de methyle

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:24889-15-4 SDS

24889-15-4Relevant articles and documents

Electrochemically induced oxidative rearrangement of alkylidenemalonates

Elinson, Michail N.,Feducovich, Sergey K.,Nikishin, Gennady I.

, p. 14529 - 14540 (2007/10/03)

Alkylidenemalonates capable of double bond migration being electrolyzed in methanol or ethanol in the presence of alkali metal halides in an undivided cell equipped with Fe cathode are transformed into 2-alkyl-3,3- dimethoxyalkane-1,2-dicarboxylates in 70-90% yield via electrochemically induced oxidative rearrangement. Acidification of the reaction mixture after the electrolysis leads to the formation of 2-alkyl-3-oxoalkane-1,1- dicarboxylates. In the case of isobutylidenemalonate, the electrolysis intermediate dimethyl 3,3-dimethyl-2-methoxy-cyclopropane-1,1-dicarboxylate was isolated in 70% yield.

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