642088-24-2

Basic information

• Product Name: 3-Isothiazolamine,N-(phenylmethyl)-,1,1-dioxide(9CI)
• Synonyms: 3-Isothiazolamine,N-(phenylmethyl)-,1,1-dioxide(9CI)
• CAS NO: 642088-24-2
• Molecular Formula: C₁₀H₁₀N₂O₂S
• Molecular Weight: 0
• Product Categories: ALCOHOL
• Mol File: 642088-24-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Isothiazolamine,N-(phenylmethyl)-,1,1-dioxide(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Isothiazolamine,N-(phenylmethyl)-,1,1-dioxide(9CI)(642088-24-2)
• EPA Substance Registry System: 3-Isothiazolamine,N-(phenylmethyl)-,1,1-dioxide(9CI)(642088-24-2)

Safety Data

• Hazardous Substances Data: 642088-24-2(Hazardous Substances Data)

Usage

Physical State

White solid

Industrial Applications

Used in pharmaceutical and agrochemical production

Antimicrobial Properties

Acts as a preservative in various products

Biocidal Activity

Controls the growth of bacteria, fungi, and algae in water-based systems

Potential Therapeutic Applications

Anti-inflammatory: Under study for anti-inflammatory properties
Anti-cancer: Shows promise in inhibiting cancer cell growth

Research Status

Further studies needed for full understanding of therapeutic potential

Upstream product

• 68449-78-5 3-(N-benzylamino)isothiazole 
• 21277-97-4 2-benzyl-2H-isothiazol-3-one 
• 2935-91-3 N,N'-Dibenzyl-3,3'-dithiobis(propionsaeureamid) 

Relevant articles and documents

Enantioselective synthesis, chiroptical properties and absolute configuration of 3-aminosubstituted isothiazole S-oxides

Herein we report a mild and efficient method to synthesize chiral 3-aminosubstituted isothiazole sulfoxides taking advantage of (+)- and (-)-((8,8-dichlorocamphoryl)sulfonyl)oxaziridine under microwave irradiation. The determination of the absolute config

Isothiazoles. Part 14: New 3-aminosubstituted isothiazole dioxides and their mono- and dihalogeno derivatives

3-Alkylamino- and 3-arylamino isothiazole dioxides unsubstituted at C-4 and C-5 were synthesized starting from dithiopropionic amides. Taking advantage of the direct chlorination during the cyclization process or realizing an addition-elimination process with bromine on the final 3-aminoisothiazole dioxide derivatives, the corresponding 5-chloro-, 4,5-dichloro- or the 4-bromoisothiazole dioxides could also be made available.