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56825-91-3

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56825-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56825-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,2 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56825-91:
(7*5)+(6*6)+(5*8)+(4*2)+(3*5)+(2*9)+(1*1)=153
153 % 10 = 3
So 56825-91-3 is a valid CAS Registry Number.

56825-91-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-dimethoxyphosphoryl-1,3-diphenylpropan-1-one

1.2 Other means of identification

Product number -
Other names dimethyl 3-oxo-1,3-diphenylpropylphosphonate

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:56825-91-3 SDS

56825-91-3Downstream Products

56825-91-3Relevant articles and documents

PS-BEMP as a basic catalyst for the phospha-Michael addition to electron-poor alkenes

Strappaveccia, Giacomo,Bianchi, Luca,Ziarelli, Simone,Santoro, Stefano,Lanari, Daniela,Pizzo, Ferdinando,Vaccaro, Luigi

supporting information, p. 3521 - 3525 (2016/04/19)

PS-BEMP was used as a heterogeneous catalyst for the phospha-Michael addition of phosphorus nucleophiles to a variety of electron-poor alkenes. The addition reactions were generally performed with equimolar amounts of reagents under solvent free conditions. The protocol proved to be very efficient for the addition to aromatic, non-aromatic and cyclic ketones, giving good yields (78-85%) in all cases. The protocol was also extended with good results to α,β-unsaturated esters and nitriles. This demonstrates that PS-BEMP is a good catalyst for the phospha-Michael addition to electron-poor alkenes.

Selective Phosphorylation of Conjugated α-Enones at the Carbonyl Group, Catalyzed by Cyclohexylamine

Galkina,Saakyan,Cherkasov,Galkin,Cherkasov,Pudovik

, p. 344 - 348 (2007/10/03)

Reaction of dialkyl phosphites with benzalacetophenone (chalcone) and benzalacetone in the presence of cyclohexylamine as a catalyst is a convenient preparative method for selective phosphorylation of conjugated α, β-unsaturated carbonyl compounds at the carbonyl group. The kinetics of cyclohexylamine-catalyzed addition of dialkyl phosphites to cis- and trans-chalcones is studied, and factors are revealed that influence the reactivity of addends in this reaction.

RATE LAWS OF THE PUDOVIK REACTION IN A SUBSTITUTED CHALCONE SERIES

Galkin, V. I.,Galkina, I. V.,Khabibullina, A. B.,Kurdi, Khalid Al,Cherkasov, R. A.,Pudovik, A. N.

, p. 290 - 292 (2007/10/02)

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