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ethyl 2-(4-fluorophenyl)-2-(hydroxyimino)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1379588-33-6

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1379588-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379588-33-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,5,8 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1379588-33:
(9*1)+(8*3)+(7*7)+(6*9)+(5*5)+(4*8)+(3*8)+(2*3)+(1*3)=226
226 % 10 = 6
So 1379588-33-6 is a valid CAS Registry Number.

1379588-33-6Relevant articles and documents

Superacid and thiol-ene reactions for access to psammaplin analogues with HDAC inhibition activities Dedicated to Professor Jean Marie Coustard, a creative chemist

El Bahhaj, Fatima,Désiré, Jér?me,Blanquart, Christophe,Martinet, Nadine,Zwick, Vincent,Sim?es-Pires, Claudia,Cuendet, Muriel,Grégoire, Marc,Bertrand, Philippe

, p. 9702 - 9708 (2014)

An innovative synthesis of psammaplin-like structure is proposed based on original methodologies using superacid, microwaves, and S-ene chemistry. The new compounds were evaluated as histone deacetylase inhibitors. The results highlight important consider

Synthesis of Air- and Moisture-Stable, Storable Chiral Oxorhenium Complexes and Their Application as Catalysts for the Enantioselective Imine Reduction

Das, Braja Gopal,Nallagonda, Rajender,Dey, Dhananjay,Ghorai, Prasanta

supporting information, p. 12601 - 12605 (2015/09/01)

Air-/moisture-stable, crystalline, and storable chiral salicyloxazoline based oxorhenium(V) complexes have been synthesized and their catalytic application for the asymmetric reduction of ketimines using hydrosilane as hydride source is disclosed. A broad substrate scope, high yields, and excellent enantioselectivities (up to 99 %) are attained. Furthermore, the syntheses of enantiopure α-amino esters, γ- and δ-lactams, and isoindolinones have also been carried out using this methodology. Finally, the method has been applied to synthetic targets of pharmaceutical relevance, such as R-(+)-salsolidine and R-(+)-crispine A.

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