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Pentanoic acid, 2-methyl-3-oxo-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26735-86-4

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26735-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26735-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,3 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26735-86:
(7*2)+(6*6)+(5*7)+(4*3)+(3*5)+(2*8)+(1*6)=134
134 % 10 = 4
So 26735-86-4 is a valid CAS Registry Number.

26735-86-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 2-methyl-3-oxopentanoate

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-oxo-valeriansaeure-tert-butylester

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:26735-86-4 SDS

26735-86-4Upstream product

26735-86-4Relevant academic research and scientific papers

A Study of the Ferrous Ion-initiated SRN1 Reactions of Halogenoarenes with tert-Butyl Acetate and N-Acylmorpholine Enolates

Leeuwen, Milko van,McKillop, Alexander

, p. 2433 - 2440 (2007/10/02)

A detailed preparative study is reported of the ferrous ion-initiated SRN1 reactions of a range of halogenoarenes with the sodium enolates of tert-butyl acetate, n-acetylmorpholine and a number of higher N-acylmorpholines.Smooth and rapid substitution occurs in many cases, and good to excellent yields were obtained of arylacetic esters or acids, arylacetamides and arylalkanamides.The broad scope and limitations of the process have been defined, and the possible role of the ferrous ion is discussed.

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