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1,2-Benzisothiazole, 2,3-dihydro-2-methyl-3-phenyl-, 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15448-92-7

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15448-92-7 Usage

Type of Compound

Heterocyclic compound

Structure

Contains a benzene ring fused to an isothiazole ring

Functionality

Acts as a strong oxidizing agent

Applications

a. Pharmaceutical production
b. Pesticide production
c. Rubber chemical production

Use as a Synthetic Intermediate

For the production of organic compounds

Biological Activity

Potential as a biological active agent

Research Areas

a. Anti-cancer activities
b. Antiviral activities

Environmental Impact

Studied for its potential toxicity and environmental effects

Check Digit Verification of cas no

The CAS Registry Mumber 15448-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15448-92:
(7*1)+(6*5)+(5*4)+(4*4)+(3*8)+(2*9)+(1*2)=117
117 % 10 = 7
So 15448-92-7 is a valid CAS Registry Number.

15448-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3-phenyl-3H-1,2-benzothiazole 1,1-dioxide

1.2 Other means of identification

Product number -
Other names ()-2-methyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide

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:15448-92-7 SDS

15448-92-7Relevant academic research and scientific papers

Structurally Diverse Synthesis of Five-, Six-, and Seven-Membered Benzosultams through Electrochemical Cyclization

Liu, Aiyun,Guo, Tiantian,Zhang, Shuangshuang,Yang, Han,Zhang, Qi,Chai, Yonghai,Zhang, Shengyong

supporting information, p. 6326 - 6331 (2021/08/23)

We have developed a metal- and oxidant-free approach to structurally diverse synthesis of benzosultams from aryl sulfonamides through an electrochemical cyclization. Upon variation of the ortho substituent on aryl sulfonamides, five-, six-, and seven-memb

Sultams: Solid phase and other synthesis of anti-HIV compounds and compositions

-

Page column 13-14, (2010/02/05)

Biologically active sultams are disclosed which have potent anti-HIV activity. A combinational method of synthesis, which uses a solid support and variants thereof, are described. Biological compositions and method of treating mammals for viral infections

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