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3H-Phenothiazine-3-one, 2-chloro-, also known as 2-Chloro-3H-phenothiazine-3-one, is a chemical compound with the molecular formula C12H8ClNO and a molecular weight of 221.65 g/mol. It is a derivative of phenothiazine, a heterocyclic compound with a tricyclic structure consisting of two benzene rings and a thiazine ring. The 2-chloro substitution introduces a chlorine atom at the 2-position of the phenothiazine core, which can significantly alter the compound's physical and chemical properties. This specific chemical is often used in the synthesis of various pharmaceuticals and dyes due to its unique reactivity and structural features. It is typically handled with care due to its potential toxicity and should be stored and used in accordance with proper safety protocols.

5964-20-5

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5964-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5964-20-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5964-20:
(6*5)+(5*9)+(4*6)+(3*4)+(2*2)+(1*0)=115
115 % 10 = 5
So 5964-20-5 is a valid CAS Registry Number.

5964-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chlorophenothiazin-3-one

1.2 Other means of identification

Product number -
Other names 2-Chlor-3-oxo-3H-phenthiazin

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:5964-20-5 SDS

5964-20-5Upstream product

5964-20-5Relevant academic research and scientific papers

Synthesis of Quinone-Imines with Iodoxybenzene

Barret, R.,Daudon, M.

, p. 1543 - 1549 (2007/10/02)

A new route to quinone-imines by using iodoxybenzene and vanadyl acetylacetonate as a catalyst is described.

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