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Benzeneacetic acid, 4-(1,1-dimethylethyl)--alpha--(1-methylethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67795-02-2

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67795-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67795-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,9 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67795-02:
(7*6)+(6*7)+(5*7)+(4*9)+(3*5)+(2*0)+(1*2)=172
172 % 10 = 2
So 67795-02-2 is a valid CAS Registry Number.

67795-02-2SDS

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 α-<4-(tert-butyl)phenyl>isovaleric acid

1.2 Other means of identification

Product number -
Other names α-[4-(tert-butyl)phenyl]isovaleric acid

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:67795-02-2 SDS

67795-02-2Downstream Products

67795-02-2Relevant academic research and scientific papers

A NEW METHOD FOR THE SYNTHESIS OF α-ARYLALKANOIC ACIDS BY THE USE OF 1,2-REARRANGEMENT OF THE ARYL GROUP

Tsuchihashi, Gen-ichi,Kitajima, Koji,Mitamura, Shuichi

, p. 4305 - 4308 (2007/10/02)

A simple synthetic method of α-arylalkanoic acids was accomplished by the use of a novel 1,2-rearrangement of the aryl group and this method was applied to the syntheses of some biologically important subtances.

Process for preparing phenyl-acetic acid esters

-

, (2008/06/13)

A process for preparing a substituted phenyl-acetic acid ester of the formula (I), SPC1 wherein R1 is an ethyl group or an isopropyl group, R2 is a hydrogen atom, a C1 -C4 alkyl group, a methoxy group, a halogen atom or a methylenedioxy group, which comprises reacting a quaternary ammonium salt of the formula (III), SPC2 wherein X is a halogen atom, and A is an alkylamine, pyridine or an N-alkylaniline, with a carboxylic acid of the formula (II), SPC3 wherein R1 and R2 are each as defined above, its reactive derivative, or a mixture of the acid and its reactive derivative.

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