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2-phenyl-1,4,5,6-tetrahydropyrimidine is a heterocyclic organic compound with the molecular formula C11H13N3. It is a derivative of pyrimidine, a six-membered aromatic ring containing four carbon atoms and two nitrogen atoms. The compound features a phenyl group (C6H5) attached to the 2-position of the pyrimidine ring, and the remaining carbon atoms are connected in a tetrahedral arrangement, forming a saturated ring structure. 2-phenyl-1,4,5,6-tetrahydropyrimidine has potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of new materials with unique properties.

5417-73-2

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5417-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5417-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5417-73:
(6*5)+(5*4)+(4*1)+(3*7)+(2*7)+(1*3)=92
92 % 10 = 2
So 5417-73-2 is a valid CAS Registry Number.

5417-73-2SDS

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-Phenyl-1,4,5,6-tetrahydropyrimidine hydrochloride

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:5417-73-2 SDS

5417-73-2Downstream Products

5417-73-2Relevant academic research and scientific papers

Synthesis of N-substituted aryl amidines by strong base activation of amines

Khalifa, Muhammad M.,Bodner, Micah J.,Berglund, J. Andrew,Haley, Michael M.

supporting information, p. 4109 - 4111 (2015/08/03)

Abstract We describe an efficient method for the direct preparation of N-substituted aryl amidines from nitriles and primary amines. The protocol employs activation of amines by a strong base and provides greater access to a pharmaceutically relevant functional group. This synthetic approach tolerates deactivated nitriles, nitriles with competing substitution sites, and aryl amines.

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