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2-Butenediamide, N-(2-chlorophenyl)-N-(2-cyanoethyl)-N',N'-dimethyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104086-51-3

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104086-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104086-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,8 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104086-51:
(8*1)+(7*0)+(6*4)+(5*0)+(4*8)+(3*6)+(2*5)+(1*1)=93
93 % 10 = 3
So 104086-51-3 is a valid CAS Registry Number.

104086-51-3SDS

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 N-(2-cyanoethyl)-N',N'-dimethyl-2'-chlorofumaranilide

1.2 Other means of identification

Product number -
Other names (E)-But-2-enedioic acid (2-chloro-phenyl)-(2-cyano-ethyl)-amide dimethylamide

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:104086-51-3 SDS

104086-51-3Downstream Products

104086-51-3Relevant academic research and scientific papers

Diastereotopic Effect of the Methylene Protons in N-ortho-Substituted-N-β-cyanoethylanilides: X-Ray Structure of N-(β-Cyanoethyl)-2'-chloromaleanilic Acid

Rodriguez, J. Gonzalez,Canoira, Laureano,Calderon, C. Esteban,Martinez-Ripoll, M.,Blanco, S. Garcia

, p. 199 - 204 (2007/10/02)

Some N-β-cyanoethyl-ortho-substituted anilides show a diastereotopic coupling effect of the methylene protons of the N-β-cyanoethyl chain in the 1H n.m.r. spectra.Resolution of those proton coupling systems have been done by computational methods and thei

Synthesis of Oxindole Derivatives from N-Alkenyl-o-Chloroanilides with Zero-Valent Nickel Complex

Canoira, L.,Rodriguez, J. G.

, p. 1511 - 1518 (2007/10/02)

Oxindole derivatives have been obtained from N-alkenyl-o-chloroanilides by reaction with tetrakis(triphenylphoaphine)nickel(0) in toluene as solvent in good yields.A detailed analysis of all the products of the reaction allows to confirm the postulated mechanism of the cyclization reaction.The o-chloroanilides of the 3-cyclohexenylacetic acid fails in the cyclization reaction, since the torsional hindrance seems to avoid that the endocyclic double bond may be orthogonally to the ortho-?-nickel complex intermediate on the aromatic ring.

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