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1025483-29-7

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1025483-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025483-29-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,4,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1025483-29:
(9*1)+(8*0)+(7*2)+(6*5)+(5*4)+(4*8)+(3*3)+(2*2)+(1*9)=127
127 % 10 = 7
So 1025483-29-7 is a valid CAS Registry Number.

1025483-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-cyano-4-phenylbutanoate

1.2 Other means of identification

Product number -
Other names methyl 2-cyano-4-phenylbutyrate

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:1025483-29-7 SDS

1025483-29-7Relevant articles and documents

EIF4E INHIBITORS AND USES THEREOF

-

Paragraph 00320; 00327, (2021/09/11)

The present invention provides compounds inhibiting elF4E activity and compositions and methods of using thereof.

Regioselective Hydrogenolysis of Donor-Acceptor Cyclopropanes with Zn-AcOH Reductive System

Ivanov, Konstantin L.,Villemson, Elena V.,Latyshev, Gennadij V.,Bezzubov, Stanislav I.,Majouga, Alexander G.,Melnikov, Mikhail Ya.,Budynina, Ekaterina M.

, p. 9537 - 9549 (2017/09/23)

A convenient low-cost method for regioselective ring-opening of donor-acceptor cyclopropanes with the Zn-AcOH reductive system was developed. The general character of the method was displayed via efficient reduction of a representative series of 2-(het)arylcyclopropane-1,1-diesters as well as donor-acceptor cyclopropanes with other types of electron-withdrawing activating groups. This method opens a rapid access to γ-substituted propyl-1,1-diesters, ketoesters, cyanoesters, cyanoamides, dinitriles, etc., many of which are not readily accessible with alternative methods. The utility of the synthesized compounds was demonstrated by transforming them into valuable acyclic and cyclic compounds (including pharmacologically relevant carbazoles, δ-lactams, and oxindole derivatives).

Atom- and step-economical preparation of reduced knoevenagel adducts using CO as a deoxygenative agent

Kolesnikov, Pavel N.,Usanov, Dmitry L.,Barablina, Evgeniya A.,Maleev, Victor I.,Chusov, Denis

supporting information, p. 5068 - 5071 (2014/12/11)

A highly efficient one-step Rh-catalyzed preparation of reduced Knoevenagel adducts of various aldehydes and ketones with active methylene compounds has been developed. The protocol does not require an external hydrogen source and employs carbon monoxide

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