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Ethenetricarbonitrile, (phenylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41996-49-0

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41996-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41996-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,9 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41996-49:
(7*4)+(6*1)+(5*9)+(4*9)+(3*6)+(2*4)+(1*9)=150
150 % 10 = 0
So 41996-49-0 is a valid CAS Registry Number.

41996-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name anilino-ethenetricarbonitrile

1.2 Other means of identification

Product number -
Other names Anilino-aethentricarbonitril

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:41996-49-0 SDS

41996-49-0Downstream Products

41996-49-0Relevant academic research and scientific papers

Hexacyanocyclopropane. II. Reaction of Hexacyanocyclopropane with Aliphatic and Aromatic Amine Hydroiodides

Nasakin,Lukin,Vershinin,Lyshchikov,Urman,Yashkanova

, p. 361 - 363 (2007/10/03)

Reaction of hexacyanocyclopropane with aliphatic amine hydroiodides gives corresponding pentacyano-2-propen-1-ides and cyanogen iodide, whereas with aromatic amine hydroiodides unsubstituted and ring-substituted N-(tricyanovinyl)anilines or N,N-dialkyl-4-(tricyanovinyl)anilines, malononitrile, and iodine are formed.

Reactions od Arylazosulfones with the Conjugate Bases of Active-Methylene Compounds

Dell'Erba, Carlo,Novi, Marino,Petrillo, Giovanni,Tavani, Cinzia

, p. 3905 - 3914 (2007/10/02)

The reaction between arylazo p-tolyl sulfones 1a-f (Ar-N=N-SO2-p-Tol) and the potassium salts of some active-methylene compounds (CH2XY: X, Y = CN, COOEt) represents an example of unprecedented behaviour of azosulfones and effectively leads, depending on the nucleophile, to either unsymmetrical (6-8) or symmetrical (9) tetrasubstituted ethylenes.Of particular interest is the possibility to synthesize, in high yields and mild conditions, polarysed ethylenes some of which are otherwise not easily accessible.A mechanism involving successive condensation processes is supported by experimental evidence.

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