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isobutyl 3,3-dimethylbutyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94021-85-9

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94021-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94021-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94021-85:
(7*9)+(6*4)+(5*0)+(4*2)+(3*1)+(2*8)+(1*5)=119
119 % 10 = 9
So 94021-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-8(2)7-12-9(11)6-10(3,4)5/h8H,6-7H2,1-5H3

94021-85-9SDS

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 2-methylpropyl 3,3-dimethylbutanoate

1.2 Other means of identification

Product number -
Other names EINECS 301-477-0

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:94021-85-9 SDS

94021-85-9Downstream Products

94021-85-9Relevant academic research and scientific papers

Improved Synthesis of Tertiary Alkylacetic Acids and Esters

Randriamahefa, S.,Deschamps, P.,Gallo, R.,Grangette, H.

, p. 493 - 495 (2007/10/02)

Tertiary alkylacetic acids (R3CCH2COOH) are prepared by reaction of 1,1-dichloroethene with a reagent capable of forming readily a tertiary alkyl carbenium ion with sulfuric acid in the absence of boron trifluoride.With tertiary butyl reagents, the yields are good and the method is convenient at laboratory and larger scales.The yields of carboxylic acids fall sharply with increasing steric effects.The esters are obtained directly, by adding alcohols, in a one-pot synthesis; with C1-C3 alcohols the reaction is selective.

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