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226-52-8

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226-52-8 Usage

Chemical family

Belongs to the phenothiazine family.

Tricyclic compound

Consists of three fused rings.

Molecular weight

284.36 g/mol.

Structure

Contains two benzene rings and a seven-membered sulfur-containing ring.

Applications

Wide range in organic chemistry and pharmaceuticals.

Building block

Used for the synthesis of various compounds with therapeutic properties.

Biological activities

Exhibits antipsychotic, antitumor, and anti-inflammatory properties.

Check Digit Verification of cas no

The CAS Registry Mumber 226-52-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,2 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 226-52:
(5*2)+(4*2)+(3*6)+(2*5)+(1*2)=48
48 % 10 = 8
So 226-52-8 is a valid CAS Registry Number.

226-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dibenzo<a,h>phenothiazine

1.2 Other means of identification

Product number -
Other names 14H-Dibenzo<a.h>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:226-52-8 SDS

226-52-8Relevant articles and documents

Organic dye sensitizer based on dibenzophenothiazine as well as preparation method and application of organic dye sensitizer

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Paragraph 0037-0041, (2021/08/07)

The invention discloses an organic dye sensitizer based on dibenzophenothiazine and a preparation method of the organic dye sensitizer; the molecule adopts alkyl chain modified triphenylamine, phenyl carbazole or indole as an electron-donating group and d

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