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1,1-Cyclopropanedicarboxylic acid, 2,2-dicyano-3-(2-fluorophenyl)-, 1,1-dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

919475-04-0

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919475-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 919475-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,4,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 919475-04:
(8*9)+(7*1)+(6*9)+(5*4)+(4*7)+(3*5)+(2*0)+(1*4)=200
200 % 10 = 0
So 919475-04-0 is a valid CAS Registry Number.

919475-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2,2-dicyano-3-(2-fluorophenyl)cyclopropane-1,1-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,2-Dicyano-3-(2-fluoro-phenyl)-cyclopropane-1,1-dicarboxylic acid dimethyl ester

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:919475-04-0 SDS

919475-04-0Downstream Products

919475-04-0Relevant academic research and scientific papers

Electrocatalytic multicomponent cyclization of aromatic aldehydes, malononitrile, and malonates into 3-substituted 2,2-dicyanocyclopropane-1,1- dicarboxylates

Vereshchagin,Elinson,Dorofeev,Nikishin

experimental part, p. 902 - 907 (2010/10/04)

Electrolysis of aromatic aldehydes, malononitrile and malonates in methanol in an undivided cell in the presence of double-mediator system NaBr-NaOAc afforded 3-substi-tuted 2,2-dicyanocyclopropane-1,1-dicarboxylates in 40-60% yields.

Stereoselective electrocatalytic cyclization of 3-substituted 2,2-dicyanocyclopropane-1,1-dicarboxylic acid esters to form 6-substituted (1R,5R,6R)*-4,4-dialkoxy-5-cyano-2-oxo-3-azabicyclo[3.1.0] hexane-1-carboxylic acid esters

Elinson,Fedukovich,Starikova,Vereshchagin,Belyakov,Gorbunov,Nikishin

, p. 106 - 111 (2007/10/03)

Electrolysis of 3-substituted 2,2-dicyanocyclopropane-1,1-dicarboxylic acid esters in alcohols in an undivided cell in the presence of NaBr or NaOAc afforded 6-substituted (1R,5R, 6R)*-4,4-dialkoxy-5-cyano-2-oxo-3- azabicyclo[3.1.0]hexane-1-carboxylic aci

Electrocatalytic multicomponent cyclization of an aldehyde, malononitrile and a malonate into 3-substituted-2,2-dicyanocyclopropane-1,1-dicarboxylate-the first one-pot synthesis of a cyclopropane ring from three different molecules

Elinson, Michail N.,Feducovich, Sergey K.,Vereshchagin, Anatolii N.,Gorbunov, Sergey V.,Belyakov, Pavel A.,Nikishin, Gennady I.

, p. 9129 - 9133 (2007/10/03)

Electrolysis of an aldehyde, malononitrile and a malonate in an alcohol in an undivided cell in the presence of sodium acetate-sodium halide as a double mediatory system results in the formation of 3-substituted-2,2-dicyanocyclopropane-1,1-dicarboxylates

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