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Bis(2-methylallyl)malonic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74793-47-8

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74793-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74793-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,9 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74793-47:
(7*7)+(6*4)+(5*7)+(4*9)+(3*3)+(2*4)+(1*7)=168
168 % 10 = 8
So 74793-47-8 is a valid CAS Registry Number.

74793-47-8SDS

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 2,2-di(2-methylallyl)malonate

1.2 Other means of identification

Product number -
Other names dimethyl 2,2-bis(2-methyl-2-propenyl)malonate

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:74793-47-8 SDS

74793-47-8Downstream Products

74793-47-8Relevant academic research and scientific papers

Platinum(IV)-Catalyzed Synthesis of Unsymmetrical Polysubstituted Benzenes via Intramolecular Cycloaromatization Reaction

Zheng, Shuyan,Zhang, Jinghua,Shen, Zhengwu

supporting information, p. 2803 - 2808 (2015/09/28)

A one-pot synthesis of polysubstituted benzene derivatives was achieved via a platinum(IV)-catalyzed intramolecular cycloaromatization reaction. The reaction proceeds via a tandem skeletal rearrangment, dehydration and double bond isomerization, which proved to be very useful for the syntheses of a range of interesting polyalkyl-substituted benzenes.

USE IN PERFUMERY AND FLAVORING AND PROCESS FOR THE PREPARATION OF 5,5-DIMETHYL-3-ETHYL-3,4-DIHYDROFURAN-2-ONE

-

Page/Page column 2, (2010/05/13)

The invention relates to the use of 5,5-dimethyl-3-ethyl-3,4-dihydrofuran-2-one (A), named “Noxolide” by the applicant, as an olfactory agent in perfumery, and also as a food flavouring. The invention also relates to a novel process for the preparation of 5,5-dimethyl-3-ethyl-3,4-dihydrofuran-2-one.

Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate

Yang, Cai-Guang,Reich, Nicholas W.,Shi, Zhangjie,He, Chuan

, p. 4553 - 4556 (2007/10/03)

(Chemical Equation Presented) Intramolecular additions of hydroxyl or carboxyl groups to inert olefins catalyzed by simple silver(I) triflate are described. Good to excellent yields can be obtained for a range of substrates under relatively mild conditions. This reaction represents one of the simplest methods to construct cyclic ethers or lactones.

Bis(aminophosphine)-nickel complexes as efficient catalysts for alkylation of allylic acetates with stabilized nucleophiles

Bricout, Herve,Carpentier, Jean-Francois,Mortreux, Andre

, p. 6105 - 6108 (2007/10/03)

The alkylation of a variety of allylic acetates with dimethyl malonate catalysed by nickel-diphosphine complexes is reported. It is shown that in most cases bis(aminophosphine) type ligands lead to much more efficient catalysts than dppb and other usual d

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