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1H-Pyrrole-3,4-dicarbonitrile, 2-amino-5-phenyl-1-[(phenylmethylene)amino]- is a complex organic compound with the molecular formula C18H13N5. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. The compound features two nitrile groups (-CN) at the 3 and 4 positions of the pyrrole ring, an amino group (-NH2) at the 2 position, and a phenyl group attached to the 5 position. Additionally, it has a phenylmethylene (C6H5-CH=) group connected to the amino group at the 1 position, forming an imine bond. 1H-Pyrrole-3,4-dicarbonitrile, 2-amino-5-phenyl-1-[(phenylmethylene)amino]- is known for its potential applications in the synthesis of various pharmaceuticals and organic materials due to its unique structure and reactivity.

85791-38-4

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85791-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85791-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,9 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85791-38:
(7*8)+(6*5)+(5*7)+(4*9)+(3*1)+(2*3)+(1*8)=174
174 % 10 = 4
So 85791-38-4 is a valid CAS Registry Number.

85791-38-4SDS

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 2-Amino-5-phenyl-1-{[1-phenyl-meth-(Z)-ylidene]-amino}-1H-pyrrole-3,4-dicarbonitrile

1.2 Other means of identification

Product number -
Other names -

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

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More Details:85791-38-4 SDS

85791-38-4Relevant academic research and scientific papers

sym-TATRACYANOETHANE IN THE SYNTHESIS OF HETEROCYCLES. 4. SYNTHESIS OF 1-ALKYLIDENEIMINO-2-AMINO-3,4,4-TRICYANO-4,5-DIHYDROPYRROLES BY THE REACTION OF sym-TETRACYANOETHANE WITH AZINES

Nasakin, O.E.,Alekseev, V.V.,Terent'ev, P.B.,Bulai, A.Kh.,Zablotskaya, M.Yu.

, p. 855 - 858 (2007/10/02)

sym-Tetracyanoethane reacts with aldazines and ketazines to give 1-alkylideneimino-2-amino-3,4,4-tricyano-4,5-dihydropyrroles, some of which are thermally converted to 1-alkylidene-2-amino-3,4-dicyanopyrroles or 5,5-disubstituted 1-alkylideneimino-2-amino

MASS-SPECTROMETRIC BEHAVIOR OF 5-SUBSTITUTED 1-ALKYLIDENEIMINO-2-AMINOPYRROLES AND THEIR 2,5- AND 4,5-DIHYDRO DERIVATIVES

Terent'ev, P.B.,Nasakin, O.E.,Alekseev, V.V.,Kalandarishvili, A.G.,Kaviladze, M.Sh.

, p. 858 - 862 (2007/10/02)

A comparative analysis of the mass spectra of 5-substituted 1-alkylideneimino-2-amino-3,4-dicyanopyrroles and their 2,5-dihydro and 4,5-dihydro derivatives makes it possible to find the typical fragmentation pathways that characterize each group of compounds and to detect the presence of tautomeric amino-imino forms in the gas phase.

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