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6-CHLORO-3-METHYL-3H-BENZOTHIAZOL-2-YLIDENEAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58199-49-8

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58199-49-8 Usage

Structure

Benzothiazole derivative with a chlorine atom and a methyl group attached to the benzothiazole ring

Uses

Reagent in organic synthesis and pharmaceutical research

Medicinal properties

Studied for potential use in the treatment of cancer and neurodegenerative disorders

Antimicrobial and antifungal activities

Investigated for its potential in these areas

Check Digit Verification of cas no

The CAS Registry Mumber 58199-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,9 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58199-49:
(7*5)+(6*8)+(5*1)+(4*9)+(3*9)+(2*4)+(1*9)=168
168 % 10 = 8
So 58199-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2S/c1-11-6-3-2-5(9)4-7(6)12-8(11)10/h2-4,10H,1H3/b10-8-

58199-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-3-methyl-1,3-benzothiazol-2-imine

1.2 Other means of identification

Product number -
Other names 6-chloro-3-methyl-3H-benzothiazol-2-one-imine

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:58199-49-8 SDS

58199-49-8Relevant academic research and scientific papers

Process for the manufacture of 2-amino-aryleno-thiazole compounds and of derivatives thereof N-substituted in the ring

-

, (2008/06/13)

2-Amino-aryleno-thiazoles in which the amino group in 2-position can be substituted by aryl, alkyl and/or cycloalkyl, and 2-imino-aryleno-thiazolines substituted at the ring nitrogen by aryl, alkyl or cycloalkyl are produced by cyclization of arylthioureas carrying corresponding substituents at the respective nitrogen atom, using thionyl chloride as cyclization agent. The advantage of the improved process resides in that the amount of sulfur formed is very low and that the other by-products are easy to separate and can be used further. The thiazoles and thiazolines are obtained in a high yield and purity. They are valuable starting compounds, especially for the manufacture of dyestuffs.

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