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Dimethyl isopropylmalonate, also known as Isopropyl dimethylmalonate, is an organic compound derived from malonic acid. It is primarily used in chemical synthesis operations and is characterized by its colorless liquid form and a mild, pleasant odor. Dimethyl isopropylmalonate is particularly significant in the pharmaceutical industry, where it plays a crucial role in drug manufacturing processes. Due to its chemical properties, handling Dimethyl isopropylmalonate requires specific safety measures to prevent discomfort and potential health hazards, such as avoiding contact with skin, eyes, inhalation, or ingestion. It is non-combustible but can decompose into hazardous products when exposed to heat.

2917-78-4

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2917-78-4 Usage

Uses

Used in Pharmaceutical Industry:
Dimethyl isopropylmalonate is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable component in the development of new drugs and the improvement of existing ones.
Used in Chemical Synthesis Operations:
Dimethyl isopropylmalonate is used as a reagent in various chemical synthesis processes. Its versatility allows it to be employed in the production of a wide range of chemical products, including polymers, dyes, and other specialty chemicals.
Used in Research and Development:
Dimethyl isopropylmalonate is utilized as a research compound in academic and industrial laboratories. Its unique properties and reactivity make it an interesting subject for studies aimed at understanding chemical reactions and developing new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 2917-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2917-78:
(6*2)+(5*9)+(4*1)+(3*7)+(2*7)+(1*8)=104
104 % 10 = 4
So 2917-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O4/c1-5(2)6(7(9)11-3)8(10)12-4/h5-6H,1-4H3

2917-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl isopropylmalonate

1.2 Other means of identification

Product number -
Other names DIMETHYL ISOPROPYLMALONATEDISCONTINUED

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:2917-78-4 SDS

2917-78-4Downstream Products

2917-78-4Relevant academic research and scientific papers

Ester derivative industrial production process

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Paragraph 0058; 0059; 0060; 0061; 0062, (2016/10/10)

The present invention provides an ester derivative industrial production process which is characterized in that a monoester or a diester derivative is obtained by reaction of a compound A and carbon monoxide or carbon dioxide under the effect of a catalyst; the production process is simple, and is different from complex production ways and demanding production conditions in the prior art, and the target ester derivative product can be synthesized by one step. The production process and synthetic routes are optimized, so that the production process is fewer in side effects, convenient in post treatment, mild in production conditions, and suitable for industrial production modes.

Hydrogenolysis of Small Cycloalkanes, XVII. - Catalytic Hydrogenation of Dimethyl Bicyclobutane-2,2-dicarboxylate

Frank, Juergen,Konrad, Gerd,Rossnagel, Ingrid,Musso, Hans,Maier, Guenther,Schwab, Wolfgang

, p. 443 - 444 (2007/10/02)

Catalytic hydrogenation of the title compound 1 yields 92-95percent of ethyl methyl malonate (2), 3-5percent of n-propyl malonate (3), 2-3percent of dimethyl 2-methyl-1,1-cyclopropanedicarboxylate (4), and no 1,1-cyclobutanedicarboxylate 5, the formation of which, however, can be induced with a poisoned catalyst.

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