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4-Pentenoic acid, 5-(2-methoxyphenyl)-2,2-dimethyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91176-34-0

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91176-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91176-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,7 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91176-34:
(7*9)+(6*1)+(5*1)+(4*7)+(3*6)+(2*3)+(1*4)=130
130 % 10 = 0
So 91176-34-0 is a valid CAS Registry Number.

91176-34-0SDS

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 (E)-5-(2-methoxyphenyl)-2,2-dimethylpent-4-enoic acid

1.2 Other means of identification

Product number -
Other names 5-(2-methoxyphenyl)-2,2-dimethylpent-4-enoic 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:91176-34-0 SDS

91176-34-0Relevant academic research and scientific papers

Highly Stereocontrolled Construction of Tricyclo1,6>dodecanes by Intramolecular Double Michael Reaction

Ihara, Masataka,Toyota, Masahiro,Abe, Mariko,Ishida, Yohhei,Fukumoto, Keiichiro,Kametani, Tetsuji

, p. 1543 - 1550 (2007/10/02)

o-Anisaldehyde has been converted, via a sigmatropic reaction and a Birch reduction, into the cyclohexenone (10) bearing an α,β-unsaturated group.Treatment of the latter with lithium hexamethyldisilazide induced an intramolecular double Michael react

STEREOCONTROLLED CONSTRUCTION OF A SPIRO FUSED BICYCLOOCTANE RING SYSTEM BY THE INTRAMOLECULAR DOUBLE MICHAEL REACTION

Ihara, Masataka,Toyota, Masahiro,Fukumoto, Keiichiro,Kametani, Tetsuji

, p. 2167 - 2170 (2007/10/02)

The lithium enolate from the cyclohexenone (8) possessing the α,β-unsaturated ester moiety caused an intramolecular double Michael reaction to produce stereoselectively the spiro fused bicyclo-octane (10).

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