35272-19-6

Usage

Uses

Used in Pharmaceutical Industry:
3-METHYL-5-NITROBENZOISOTHIAZOLE is used as a key intermediate in the synthesis of various drugs, contributing to the development of new medications with improved therapeutic properties. Its unique chemical structure allows for the creation of diverse pharmaceutical compounds with potential applications in treating a wide range of diseases and medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 3-METHYL-5-NITROBENZOISOTHIAZOLE is utilized as a precursor in the production of various agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds enhances their effectiveness in controlling pests and weeds, thereby improving crop yields and ensuring food security.
Used in Organic Synthesis:
3-METHYL-5-NITROBENZOISOTHIAZOLE also serves as a valuable reagent in organic synthesis, enabling the formation of complex organic molecules through a series of chemical reactions. Its presence in these reactions facilitates the synthesis of advanced organic compounds with specific properties and applications in various industries, including materials science, polymer chemistry, and specialty chemicals.
Overall, 3-METHYL-5-NITROBENZOISOTHIAZOLE is a versatile and essential chemical compound with a wide range of applications across different industries, particularly in the development and production of pharmaceuticals, agrochemicals, and other organic compounds. Its unique structure and properties make it a valuable asset in the field of chemical synthesis and research.

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 academic research and scientific papers

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

A convenient approach towards 2- and 3-aminobenzo[b]thiophenes

Reaction of 1-(2-chloro-5-nitrophenyl)ethanone via Willgerodt-Kindler route with primary or secondary amines and sulfur allows a simple, efficient one-pot synthesis of 3-aminobenzo[b]thiophenes. Base-catalyzed transformation of 4-(2-chloro-5-nitrophenyl)-

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).

Processes and intermediate compounds for the preparation of 2-(N,N-disubstituted) amino-4-(perfluoroalkyl)-1, 3- oxazin-6-one and 6-(perfluoroalkyl) uracil compounds

An improved process and intermediate compounds for the preparation of 2-(N,N-disubstituted)amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds having the structural formula I and an improved process for the preparation of 6-(perfluoroalkyl)uracil compound

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.

Process for the preparation of 6-(perfluoroalkyl) uracil compounds form urea compounds

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

Process for the preparation of 6-(perfluoroalkyl) uracil compounds from 2-(N,N-disubstituted) amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds

An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having the structural formula I from 2-(N,N-disubstituted)amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds having the structural formula II

3-(1,2-benzisothiazol- and isoxazol-5-Y1)-2,4(1H,3H)-pyrimidinedione or thione and 3-(1,2-benzisothiazol- and isoxazol-5-y1)-4(3H)-pyrimidinone or thione herbicidal agents

There are provided 3-(1,2-benzisothiazol- and isoxazol-5-yl)-2,4(1H,3H)-pyrimidinedione or thione compounds of formula I and 3-(1,2-benzisothiazol- and isoxazol-5-yl)-4(3H)-pyrimidinone or thione compounds of formula II Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.

Substituted benzisoxazole and benzisothiazole herbicidal agents

There are provided substituted benzisoxazole and benzisothiazole compounds having the structural formula I STR1 Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.

Condensed Isothiazoles. Part 7. Substitution Reactions of 3-Methyl-1,2-benzisothiazole and Some of Its 4- and 5-Substituted Derivatives

Some electrophilic substitution reactions of 3-methyl-1,2-benzisothiazole and its 4-bromo-, 5-acetamido-, 5-amino, 5-bromo-, 5-hydroxy-, and 5-methoxy-derivatives are described. 4-Chloro, 4-bromo-, 4,6-dibromo- and 4-nitro-3-methyl-1,2-benzisothiazole may be obtained by deamination of the appropriate substitution products of 5-amino-3-methyl-1,2-benzisothiazole.Improved syntheses of 7-chloro- and 7-bromo-3-methyl-1,2-benzisothiazole have been achieved.