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Methylmalonic acid dibutyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52886-83-6

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52886-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52886-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52886-83:
(7*5)+(6*2)+(5*8)+(4*8)+(3*6)+(2*8)+(1*3)=156
156 % 10 = 6
So 52886-83-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O4/c1-4-6-8-15-11(13)10(3)12(14)16-9-7-5-2/h10H,4-9H2,1-3H3

52886-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl-malonic acid dibutyl ester

1.2 Other means of identification

Product number -
Other names 2-Methyl-malonic acid dibutyl ester

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:52886-83-6 SDS

52886-83-6Downstream Products

52886-83-6Relevant academic research and scientific papers

Copper-Catalyzed Dehydrogenative Diels-Alder Reaction

Jiang, Bing,Liang, Qiu-Ju,Han, Yu,Zhao, Meng,Xu, Yun-He,Loh, Teck-Peng

supporting information, p. 3215 - 3219 (2018/06/11)

A practical and effective copper-catalyzed dehydrogenative Diels-Alder reaction of gem-diesters and ketone with dienes has been established. The active dienophiles were generated in situ via a radical-based dehydrogenation process, which reacted with a wide variety of dienes to afford various polysubstituted cyclohexene derivatives in good to excellent yields.

Efficient synthesis of dissymmetric malonic acid S, O -esters via monoalcoholysis of symmetric dithiomalonates under neutral conditions

Matsuo, Kazumasa,Shindo, Mitsuru

supporting information; experimental part, p. 4406 - 4409 (2011/10/08)

A novel method for the highly selective synthesis of dissymmetric S,O-malonates starting from symmetric diphenyl dithiomalonates under neutral conditions is described. The key step is the thermal formation of an acylketene, the stability of which would co

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