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26278-83-1

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26278-83-1 Usage

General Description

(2-AMINO-4,7-DIMETHYL)BENZOTHIAZOL-6-OL, HCL is a chemical compound with a molecular formula C11H14ClNOS. It is a heterocyclic organic compound containing a benzothiazole ring, an amino group, and a hydroxyl group. The hydrochloride salt form of this compound is commonly used in the pharmaceutical industry as a potential anti-cancer agent, as it has been found to exhibit cytotoxic and apoptosis-inducing activities in cancer cells. Additionally, it has shown potential in inhibiting the growth of leukemia and solid tumors. (2-AMINO-4,7-DIMETHYL)BENZOTHIAZOL-6-OL, HCL is a promising compound for further research and development in the treatment of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 26278-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,7 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26278-83:
(7*2)+(6*6)+(5*2)+(4*7)+(3*8)+(2*8)+(1*3)=131
131 % 10 = 1
So 26278-83-1 is a valid CAS Registry Number.

26278-83-1SDS

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-amino-4,7-dimethyl-1,3-benzothiazol-6-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-4,7-dimethyl-6-hydroxybenzothiazole hydrochloride monohydrate

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:26278-83-1 SDS

26278-83-1Relevant articles and documents

Novel dual inhibitors of 5-lipoxygenase and thromboxane A2 synthetase: Synthesis and structure-activity relationships of 3-pyridylmethyl-substituted 2-amino-6-hydroxybenzothiazole derivatives

Hibi,Okamoto,Tagami,Numata,Kobayashi,Shinoda,Kawahara,Murakami,Oketani,Inoue,Shibata,Yamatsu

, p. 3062 - 3070 (2007/10/02)

As part of our search for novel antiinflammatory drug candidates, we have designed and synthesized a series of 3-pyridylmethyl-substituted 2-amino-6- hydroxybenzothiazoles. Introduction of a 3-pyridylmethyl group into the 2- amino group (type-A) or the be

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