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2-Amino-6-methyl-4,6-diphenyl-2,4-cyclohexadiene-1,1,3-tricarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71908-64-0

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71908-64-0 Usage

Chemical compound

2-Amino-6-methyl-4,6-diphenyl-2,4-cyclohexadiene-1,1,3-tricarbonitrile

Derivative

Tricarbonitrile

Structure

Contains a cyclohexadiene ring with two phenyl and one methyl substituents

Functional group

Amino group

Potential applications

Organic synthesis, pharmaceuticals, material science
Complex structure

Potential toxicity

Further research needed to fully understand properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 71908-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,0 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71908-64:
(7*7)+(6*1)+(5*9)+(4*0)+(3*8)+(2*6)+(1*4)=140
140 % 10 = 0
So 71908-64-0 is a valid CAS Registry Number.

71908-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-methyl-4,6-diphenylcyclohexa-2,4-diene-1,1,3-tricarbonitrile

1.2 Other means of identification

Product number -
Other names 2-Amino-6-methyl-4,6-diphenyl-2,4-cyclohexadiene-1,1,3-tricarbonitrile

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:71908-64-0 SDS

71908-64-0Relevant academic research and scientific papers

Imidazole-mediated cascade [2 + 2 + 2] annulation reactions: A highly diastereoselective synthetic protocol for the construction of multiply substituted cyclohexanes

Liu, Xu-Guang,Shi, Min

scheme or table, p. 6168 - 6174 (2009/05/27)

A novel imidazole-mediated [2 + 2 + 2] annulation process that enables the diastereoselective synthesis of multiply substituted cyclohexanes 3 in a one-pot, three-component manner from two units of (arylmethylidene) malononitriles 1 and one unit of nitroalkenes 2 is described. These cyclohexane derivatives were obtained in moderate to good yields under mild conditions. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

SYNTHESIS AND CHEMICAL REACTIVITY OF 4,4-DISUBSTITUTED PYRANAMINES

Martin-Leon, Nazario,Segura, Jose L.,Seoane, Carlos,Soto, Jose L.

, p. 2434 - 2452 (2007/10/02)

The synthesis of a variety of 4,4-disubstituted 4H-pyranamines from alkylarylpropenenitriles and benzoylacetonitrile is reported.The reaction requirements demanded a different approach from the general synthesis of 2-amino-4H-pyrans.Electronic and steric

DIMERIZATION OF 2-ARYLPROPENE-1,1-DICARBONITRILES

Abramenko, Yu. T.,Ivashchenko, A. V.,Nogaeva, K. A.,Andronova, N. A.,Putsykina, E. B.

, p. 230 - 235 (2007/10/02)

The base-catalyzed dimerization of 2-arylpropene-1,1-dicarbonitriles to 2-amino-4,6-diaryl-5-methyl-2,4-cyclohexadiene-1,1,3-tricarbonitriles and also the recyclization of the latter to 4,6-diaryl-6-methyl-2-dicyanomethylene-1,2,5,6-tetrahydronicotinonitr

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