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4-Benzothiazolamine,5-methoxy-2-methyl-(9CI) is a heterocyclic aromatic compound belonging to the benzothiazoles class, characterized by a benzene ring fused to a thiazole ring. This specific derivative features a methyl group at the 2-position and a methoxy group at the 5-position, and is recognized for its potential applications in chemical synthesis and medicinal chemistry research due to its unique structure and properties.

265312-59-2

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265312-59-2 Usage

Uses

Used in Chemical Synthesis:
4-Benzothiazolamine,5-methoxy-2-methyl-(9CI) serves as a building block in the synthesis of other organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 4-Benzothiazolamine,5-methoxy-2-methyl-(9CI) is utilized for its potential biological and pharmacological properties, making it a valuable compound in the discovery and development of new drugs. Its specific structure positions it as a candidate for further exploration in medicinal chemistry research to understand and harness its potential therapeutic effects.
While the provided materials do not detail specific applications or industries for 4-Benzothiazolamine,5-methoxy-2-methyl-(9CI) beyond its use as a building block in chemical synthesis and its potential in pharmaceutical applications, it is important to note that further studies are necessary to fully explore and understand its uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 265312-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,5,3,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 265312-59:
(8*2)+(7*6)+(6*5)+(5*3)+(4*1)+(3*2)+(2*5)+(1*9)=132
132 % 10 = 2
So 265312-59-2 is a valid CAS Registry Number.

265312-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-2-methyl-1,3-benzothiazol-4-amine

1.2 Other means of identification

Product number -
Other names 5-METHOXY-2-METHYLBENZO[D]THIAZOL-4-AMINE

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:265312-59-2 SDS

265312-59-2Relevant academic research and scientific papers

Benzimidazole- and benzothiazole-quinones: Excellent substrates for NAD(P)H:quinone oxidoreductase 1

Newsome, Jeffery J.,Colucci, Marie A.,Hassani, Mary,Beall, Howard D.,Moody, Christopher J.

, p. 3665 - 3673 (2008/09/21)

A series of benzimidazole- and benzothiazole-quinones has been synthesized. The ability of these heterocyclic quinones to act as substrates for recombinant human NAD(P)H:quinone oxidoreductase (NQO1), a two-electron reductase upregulated in tumour cells,

Synthesis and biological evaluation of novel heterocyclic quinones as inhibitors of the dual specificity protein phosphatase CDC25C

Lavergne, Olivier,Fernandes, Anne-Cecile,Brehu, Laetitia,Sidhu, Alban,Brezak, Marie-Christine,Prevost, Gregoire,Ducommun, Bernard,Contour-Galcera, Marie-Odile

, p. 171 - 175 (2007/10/03)

A focused set of heterocyclic quinones based on the benzothiazole, benzoxazole, benzimidazole, indazole and isoindole was prepared and screened with respect to the inhibition of the phosphatase activity of CDC25C. Benzoxazole- and benzothiazole-diones wer

5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents

Ryu, Chung-Kyu,Kang, Hye-Young,Lee, Sang Kook,Nam, Kyung Ae,Hong, Chang Yong,Ko, Won-Gil,Lee, Byung-Hoon

, p. 461 - 464 (2007/10/03)

5-Arylamino-2-methyl-4,7-dioxobenzothiazoles were synthesized as inhibitors of cyclin-dependent kinase 4 (CDK4) and cytotoxic agents. Most of the 4,7-dioxobenzothiazoles exhibited selective inhibitory activities for the CDK4 and cytotoxic potential agains

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