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27922-90-3

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27922-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27922-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27922-90:
(7*2)+(6*7)+(5*9)+(4*2)+(3*2)+(2*9)+(1*0)=133
133 % 10 = 3
So 27922-90-3 is a valid CAS Registry Number.

27922-90-3SDS

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 1,2-bis(3,4-dimethoxyphenyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names -

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:27922-90-3 SDS

27922-90-3Downstream Products

27922-90-3Relevant articles and documents

PCP-Bis(phosphinite) pincer complexes: new homogeneous catalysts for α-arylation of ketones

Churruca, Fátima,SanMartin, Raul,Tellitu, Imanol,Domínguez, Esther

, p. 3233 - 3237 (2007/10/03)

Two new p-alkoxycarbonylated palladium bis(phosphinite) PCP pincer complexes are easily prepared and for the first time evaluated as homogeneous catalysts in α-arylation of ketone enolates. Apart from the total absence of phenyl-aryl exchange by-products and significantly low catalyst loadings, the general α-arylation protocols described in this letter feature not only a broad applicability to a range of ketones and aryl bromides with marked electronic and steric differences but also the possibility to generate mono-diarylated products.

Palladium-catalyzed arylation of ketone enolates: an expeditious entry to tamoxifen-related 1,2,2-triarylethanones.

Churruca, Fatima,SanMartin, Raul,Tellitu, Imanol,Dominguez, Esther

, p. 1591 - 1594 (2007/10/03)

[reaction: see text]. After a rigorous study on the effect of several catalytic systems, a simple, high yielding procedure for the preparation of 1,2,2-triarylethanones, skeletal analogues of tamoxifen, is presented. Apart from the economic and environmen

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