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The chemical compound "5-(1,3-benzothiazol-2(3H)-ylidene)-6-[4-(diethylamino)phenyl]-4-phenyl-5,6-dihydropyrimidin-2(1H)-one" is a complex organic molecule with a unique structure. It features a pyrimidin-2(1H)-one core, which is a heterocyclic ring system containing both nitrogen and carbon atoms. The compound is characterized by a 1,3-benzothiazole group attached to the 5-position of the pyrimidine ring, which contributes to its electronic properties. Additionally, it has a diethylamino group at the 4-position of a phenyl ring that is connected to the 6-position of the pyrimidine, enhancing its solubility and potentially its biological activity. The presence of phenyl groups at the 4-position of the pyrimidine and the 4-position of the diethylaminophenyl ring provides further structural complexity and may influence the compound's interactions with other molecules. 5-(1,3-benzothiazol-2(3H)-ylidene)-6-[4-(diethylamino)phenyl]-4-phenyl-5,6-dihydropyrimidin-2(1H)-one is of interest in the field of medicinal chemistry due to its potential applications as a pharmacophore or a building block for the development of new drugs.

6543-17-5

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6543-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6543-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6543-17:
(6*6)+(5*5)+(4*4)+(3*3)+(2*1)+(1*7)=95
95 % 10 = 5
So 6543-17-5 is a valid CAS Registry Number.

6543-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3H-1,3-benzothiazol-2-ylidene)-6-[4-(diethylamino)phenyl]-4-phenyl-1,6-dihydropyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 2,2-Diethyl-1,3-dioxan

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 -
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More Details:6543-17-5 SDS

6543-17-5Relevant academic research and scientific papers

Recognition of cyclic, acyclic, exocyclic, and spiro acetals via structurally diagnostic ion/molecule reactions with the (CH3) 2N-C+=O acylium ion

Benassi, Mario,Moraes, Luiz Alberto B.,Cabrini, Liliane G.,Dias, Luiz Carlos,Aguilar, Andrea M.,Romeiro, Gilberto A.,Eberlin, Livia S.,Eberlin, Marcos N.

, p. 5549 - 5557 (2008/12/20)

(Chemical Equation Presented) Reactions of the model acylium ion (CH 3)2N-C+=O with acyclic, exocyclic, and spiro acetals of the general formula R1O-CR3R 4-OR2 were systematically evaluated via pentaquadrupole mass spectrometry. Characteristic intrinsic reactivities were observed for each of these classes of acetals. The two most common reactions observed were hydride and alkoxy anion [R1O- and R2O-] abstraction. Other specific reactions were also observed: (a) a secondary polar [4+ + 2] cycloaddition for acetals bearing α,β-unsaturated R3 or R4 substituents and (b) OH- abstraction for exocyclic and spiro acetals. These structurally diagnostic reactions, in conjunction with others observed previously for cyclic acetals, are shown to reveal the class of the acetal molecule and its ring type and substituents and to permit their recognition and distinction from other classes of isomeric molecules.

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