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2-(4-chlorophenyl)-6-hydroxy-4H-1,3-thiazin-4-one is a chemical compound with the molecular formula C9H5ClNOS. It is a derivative of 1,3-thiazine, a heterocyclic compound consisting of a six-membered ring with one sulfur atom and one nitrogen atom. The structure features a 4-chlorophenyl group at the 2-position, a hydroxyl group at the 6-position, and a carbonyl group at the 4-position. 2-(4-chlorophenyl)-6-hydroxy-4H-1,3-thiazin-4-one may have potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. However, its specific uses and properties depend on further research and characterization.

1433-65-4

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1433-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1433-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1433-65:
(6*1)+(5*4)+(4*3)+(3*3)+(2*6)+(1*5)=64
64 % 10 = 4
So 1433-65-4 is a valid CAS Registry Number.

1433-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-6-hydroxy-1,3-thiazin-4-one

1.2 Other means of identification

Product number -
Other names HMS1366D19

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:1433-65-4 SDS

1433-65-4Relevant academic research and scientific papers

Azines and azoles. C. Structure of 2-aryl-1,3-thiazinediones in solutions

Kuklin,Yakovlev,Smorygo,Strelkova,Ivin

, p. 985 - 997 (2007/10/03)

According to the 1H and 13C NMR, IR, and UV spectra of solutions of potentially tautomeric 2-aryl-1,3-thiazine-4,6-diones and compounds with fixed structures, modeling all possible tautomeric forms, in nonpolar and dipolar aprotic solvents, alcohols, and aqueous-alcoholic media at pH2, a mixture of the 4-hydroxy enol with corresponding anion (pKa 3.6-5.1, 40% aqueous ethanol) occurs. The experimental results are supported by PPP quantum-chemical calculations.

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