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84118-71-8

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84118-71-8 Usage

Physical state

Yellow solid

Solubility

Insoluble in water, soluble in organic solvents (e.g., ethyl acetate and acetone)

Uses

a. Precursor in the synthesis of various organic compounds
b. Synthesis of pharmaceuticals and dyes
c. Ligand in coordination chemistry for forming metal complexes

Potential applications

a. Materials science
b. Development of light-emitting and optoelectronic devices

Check Digit Verification of cas no

The CAS Registry Mumber 84118-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,1 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84118-71:
(7*8)+(6*4)+(5*1)+(4*1)+(3*8)+(2*7)+(1*1)=128
128 % 10 = 8
So 84118-71-8 is a valid CAS Registry Number.

84118-71-8SDS

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 (E)-1,3-bis(2-methylphenyl)but-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1,3-bis(2-methylphenyl)-2-butene-1-one

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:84118-71-8 SDS

84118-71-8Downstream Products

84118-71-8Relevant articles and documents

Palladium-Catalyzed Acylation of Unsaturated Halides by Anions of Enol Ethers

Russell, Charles E.,Hegedus, Louis S.

, p. 943 - 949 (2007/10/02)

Zinc salts of enol ether anions are coupled to aryl and alkenyl halides by using palladium catalysts, effecting a direct acetylation of aryl and alkenyl halides.Zinc salts of allenic ethers are coupled with aryl and alkenyl halides under similar conditions to give α,β-unsaturated ketones, the allenic ether serving as a source of the acryloyl group.Allenic ethers were γ arylated in a palladium-catalyzed coupling with aryl halides to give β,β-diaryl-α,β-unsaturated aldehydes.

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