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119591-34-3

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119591-34-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The chemical structure describes the arrangement of atoms and the types of bonds between them in the compound.

Explanation

A preservative is a substance that is added to products to prevent spoilage, deterioration, or contamination.

Explanation

The compound is utilized in different industries for its antimicrobial properties, which help maintain the quality and longevity of products.

Explanation

The compound has the ability to kill or inhibit the growth of microorganisms, making it useful in controlling microbial contamination.

Explanation

The compound's antimicrobial and antifungal properties make it suitable for use in these industries to prevent the growth of harmful microorganisms.

Explanation

Due to its antimicrobial and antifungal properties, the compound may have potential uses in these industries for the development of new drugs or treatments.

Explanation

This is the IUPAC name of the compound, which provides a standardized way to identify and refer to the chemical.

Explanation

Synonyms are alternative names for a compound, which can be useful for searching or identifying the substance in different contexts.

Explanation

Physical properties such as color, state (solid, liquid, or gas), melting point, boiling point, and solubility are not mentioned in the material provided.

Chemical structure

Heterocyclic compound with a benzene ring fused to an isothiazole ring and a sulfur dioxide group.

Type of compound

Preservative

Industrial applications

Used in the production of various consumer products.

Antimicrobial properties

Acts as a biocide and fungicide.

Common uses

In the manufacturing of paints, adhesives, and metalworking fluids.

Potential applications

Pharmaceutical and agricultural industries.

Synonyms

Not provided in the material.

Physical properties

Not provided in the material.

Check Digit Verification of cas no

The CAS Registry Mumber 119591-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,9 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119591-34:
(8*1)+(7*1)+(6*9)+(5*5)+(4*9)+(3*1)+(2*3)+(1*4)=143
143 % 10 = 3
So 119591-34-3 is a valid CAS Registry Number.

119591-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-iodobenzo[d]isothiazol-3(2H)-one 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 6-iodo-1,1-dioxo-1λ6-benz[d]isothiazol-3-one

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:119591-34-3 SDS

119591-34-3Relevant articles and documents

A convenient synthesis of 2-methoxycarbonyl-5-iodobenzene sulfonamide

Cai, Xinhong,Chen, Qiulu,Guan, Jing,Gong, Shunze,Fu, Hao,Xu, Defeng

, p. 1622 - 1624 (2017)

A convenient and concise synthesis of 2-methyl-5-nitrobenzene sulfonamide can be achieved by sulfochlorination and ammoniation with p-nitrotoluene as raw materials for an 81.2 % yield. 6-Aminosaccharin can be produced via oxidation and reduction in a 64.3

Design, synthesis and preliminary bioactivity studies of 1,2-dihydrobenzo[d]isothiazol-3-one-1,1-dioxide hydroxamic acid derivatives as novel histone deacetylase inhibitors

Han, Leiqiang,Wang, Lei,Hou, Xuben,Fu, Huansheng,Song, Weiguo,Tang, Weiping,Fang, Hao

, p. 1529 - 1538 (2014/03/21)

Histone deacetylase (HDAC) is a clinically validated target for antitumor therapy. In order to increase HDAC inhibition and efficiency, we developed a novel series of saccharin hydroxamic acids as potent HDAC inhibitors. Among them, compounds 11e, 11m, 11

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