35272-19-6

Basic information

• Product Name: 3-METHYL-5-NITROBENZOISOTHIAZOLE
• Synonyms: 3-METHYL-5-NITROBENZOISOTHIAZOLE;3-[(3-Methyl-5-nitrophenyl)Methyl]-1,2-thiazole;3-Methyl-5-nitrobenzo[d]isothiazole
• CAS NO: 35272-19-6
• Molecular Formula: C8H6N2O2S
• Molecular Weight: 194.21
• Product Categories: pharmacetical
• Mol File: 35272-19-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 260.6 °C at 760 mmHg
• Flash Point: 111.4 °C
• Appearance: /
• Density: 1.445 g/cm³
• Vapor Pressure: 0.0196mmHg at 25°C
• Refractive Index: 1.7
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-METHYL-5-NITROBENZOISOTHIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHYL-5-NITROBENZOISOTHIAZOLE(35272-19-6)
• EPA Substance Registry System: 3-METHYL-5-NITROBENZOISOTHIAZOLE(35272-19-6)

Safety Data

• Hazardous Substances Data: 35272-19-6(Hazardous Substances Data)

Usage

General Description

3-Methyl-5-nitrobenzoisothiazole is a chemical compound used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is a heterocyclic compound, meaning it contains one or more non-carbon atoms in the ring structure, with a nitro group and a methyl group attached to the benzene ring. 3-METHYL-5-NITROBENZOISOTHIAZOLE may be used as a building block in the production of drugs or as a reagent in organic synthesis. Its precise applications and properties depend on the specific chemical reactions and processes in which it is used.

InChI:InChI=1/C8H6N2O2S/c1-5-7-4-6(10(11)12)2-3-8(7)13-9-5/h2-4H,1H3

Upstream product

• 6187-89-9 3-methyl-1,2-benzisothiazole 
• 23082-50-0 2'-chloro-5'-nitroacetophenone 

Downstream Products

• 73437-03-3 5-amino-3-methyl-1,2-benzisothiazole 

Relevant articles and documents

One-pot synthesis of substituted 2-aminobenzo[b]thiophenes

(Chemical Equation Presented) Reaction of 1-(2-chloro-5-nitrophenyl) ethanone 1, via Willgerodt-Kindler routes, using the primary and secondary amines 2a-k resulted in a simple, efficient three-component one-pot synthesis of 2-aminobenzo[b]thiophenes 3a-k

PROCESS FOR THE PREPARATION OF 6-(PERFLUOROALKYL)URACIL COMPOUNDS FROM CARBAMATE COMPOUNDS

An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having structural formula (I) from carbamate compounds having structural formula (II).

Herbicidal 3 -heterocyclic substituted benzisothiazole and benzisoxazole compounds

There are provided 3-heterocyclic substituted benzisothiazole and benzisoxazole compounds having the structural formula I where Q, X, X1 and Z are defined as in claim 1. Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.