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2-(1-amino-2-benzoyl-3-oxobut-1-en-1-yl)-5-benzoyl-6-methylpyrimidine-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79593-43-4

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79593-43-4 Usage

Molecular structure

2-(1-amino-2-benzoyl-3-oxobut-1-en-1-yl)-5-benzoyl-6-methylpyrimidine-4-carboxamide is a complex organic compound containing a pyrimidine ring with various substituents.

Pyrimidine ring

The core structure of the compound is a pyrimidine ring, which is a six-membered aromatic heterocyclic ring consisting of four carbon atoms and two nitrogen atoms.

Benzoyl group at the 5th position

A benzoyl group (C6H5CO-) is attached to the pyrimidine ring at the 5th position, which is a phenyl group connected to a carbonyl group.

Methyl group at the 6th position

A methyl group (CH3) is attached to the pyrimidine ring at the 6th position, contributing to the compound's structure and properties.

Amino group linked to a benzoyl group

The compound features an amino group (NH2) connected to a benzoyl group, which may contribute to its potential biological activity.

3-oxobut-1-en-1-yl moiety

A 3-oxobut-1-en-1-yl group (CH2CH=CHCOCH3) is present in the compound, adding to its complexity and potential reactivity.

Carboxamide group at the 4th position

A carboxamide group (CONH2) is attached to the pyrimidine ring at the 4th position, which may contribute to the compound's solubility and hydrogen bonding properties.

Potential biological activity

The complex structure of the compound suggests that it may have potential biological activity, making it a candidate for pharmaceutical research and drug development.

Need for further studies

To fully understand the properties and potential applications of 2-(1-amino-2-benzoyl-3-oxobut-1-en-1-yl)-5-benzoyl-6-methylpyrimidine-4-carboxamide, additional research and experimentation are required.

Check Digit Verification of cas no

The CAS Registry Mumber 79593-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79593-43:
(7*7)+(6*9)+(5*5)+(4*9)+(3*3)+(2*4)+(1*3)=184
184 % 10 = 4
So 79593-43-4 is a valid CAS Registry Number.

79593-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(E)-1-amino-2-benzoyl-3-oxobut-1-enyl]-5-benzoyl-6-methylpyrimidine-4-carboxamide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79593-43-4 SDS

79593-43-4Downstream Products

79593-43-4Relevant academic research and scientific papers

SYNTHESIS OF PYRIMIDINES FROM β-DICARBONYL COMPOUNDS AND CYANOGEN: A METAL-CATALYSED ONE-POT PROCESS.

Basato, Marino,Corain, Benedetto,Marcomini, Antonio,Valle, Giovanni,Zanotti, Giuseppe

, p. 965 - 974 (2007/10/02)

Highly functionalized pyrimidines can be prepared in good yields, by a one-pot procedure, from cyanogen and β-dicarbonyl compounds at ambient conditions in dichloroethane in the presence of catalytic amounts of Ni(acac)2 or Cu(acac)2.The pyrimidines obtai

Metal-Catalyzed Synthesis of Cyano Enaminediones from β-Dicarbonyl Compounds and Cyanogen. Identification of Traube's Isomers

Basato, M.,Corain, B.,Veronese, A. C.,D'Angeli, F.,Valle, G.,Zanotti, G.

, p. 4696 - 4700 (2007/10/02)

Bis(2,4-pentanedionato)zinc(II) is found to be a mild, efficient, and simple to use catalyst for the additions of a variety of β-dicarbonyls to cyanogen in aprotic solvents.The catalytic system is very selective in the formation of multifunctional cyano e

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