85392-01-4

Basic information

• Product Name: 4-CHLORO-2-(CHLOROSULFONYL) BENZOIC ACID METHYL ESTER
• Synonyms: 4-CHLORO-2-(CHLOROSULFONYL) BENZOIC ACID METHYL ESTER;methyl 4-chloro-2-(chlorosulphonyl)benzoate;methyl 4-chloro-2-(chlorosulfonyl)benzoate;Einecs 286-858-9;4-CHLORO-2-(CHLOROSU
• CAS NO: 85392-01-4
• Molecular Formula: C8H6Cl2O4S
• Molecular Weight: 269.1
• EINECS: 286-858-9
• Mol File: 85392-01-4.mol

Chemical Properties

• Boiling Point: 376 °C at 760 mmHg
• Flash Point: 181.2 °C
• Appearance: /
• Density: 1.529 g/cm³
• Vapor Pressure: 7.49E-06mmHg at 25°C
• Refractive Index: 1.553
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-CHLORO-2-(CHLOROSULFONYL) BENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-2-(CHLOROSULFONYL) BENZOIC ACID METHYL ESTER(85392-01-4)
• EPA Substance Registry System: 4-CHLORO-2-(CHLOROSULFONYL) BENZOIC ACID METHYL ESTER(85392-01-4)

Safety Data

• Hazardous Substances Data: 85392-01-4(Hazardous Substances Data)

Usage

Uses

Used in Agricultural Industry:
4-Chloro-2-(chlorosulfonyl) benzoic acid methyl ester is used as a herbicide and pesticide for its ability to inhibit the growth of unwanted plants and pests. It is particularly effective in controlling a wide range of plant species and pests, thereby protecting crops and improving agricultural productivity.
Used in Chemical Synthesis:
In the chemical industry, 4-chloro-2-(chlorosulfonyl) benzoic acid methyl ester serves as an intermediate in the synthesis of various organic compounds. Its unique functional groups make it a versatile building block for the development of new chemical entities with potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science.
Used in Environmental Management:
4-Chloro-2-(chlorosulfonyl) benzoic acid methyl ester can be utilized in environmental management applications, such as the remediation of contaminated soils and water bodies. Its ability to target and inhibit the growth of unwanted organisms makes it a potential tool for addressing environmental challenges related to invasive species and pollution.

InChI:InChI=1/C8H6Cl2O4S/c1-14-8(11)6-3-2-5(9)4-7(6)15(10,12)13/h2-4H,1H3

Upstream product

• 89-77-0 2-Amino-4-chlorobenzoic acid 
• 5900-58-3 2-amino-4-chloro-benzoic acid methyl ester 
• 107-06-2 1,2-dichloro-ethane 

Downstream Products

• 914221-64-0 4-chloro-2-(N-methyl-N-phenylaminesulfonyl)benzoic acid methyl ester 
• 208465-21-8 mesosulfuron-methyl 
• 52948-12-6 Methyl 4-chloro-2-mercaptobenzoate 
• 46149-10-4 6-chloro-1,2-benzisothiazol-3(2H)-one 1,1-dioxide 

Relevant articles and documents

Synthetic method of 4-chloro-2-(N-methyl-N-phenyl sulfamoyl) methyl benzoate

The invention provides a synthetic method of 4-chloro-2-(N-methyl-N-phenyl sulfamoyl) methyl benzoate. The technical scheme is that 4-chloro-2-aminobenzoic acid is taken as a raw material and has an esterification reaction, a product is subjected to diazotization and the Sandmeyer reaction, methyl 4-chloro-2-(chlorosulfonyl)benzoate is prepared and subjected to condensation with N-methylaniline, and 4-chloro-2-(N-methyl-N-phenyl sulfamoyl) methyl benzoate is obtained. The synthetic method has the advantages of conciseness, high efficiency, mild conditions, no need of purification of an intermediate and simple operation, the total yield of three steps of reactions is as high as 65%, and the method is quite suitable for industrial production.

A method for preparing the methyl two sulphur are prosperous (by machine translation)

The invention discloses a method for synthesizing the methyl two sulphur are prosperous, belongs to the pesticide chemical field, the synthetic method is to 4 - chloro - 2 - aminobenzoic acid as the raw materials, by esterification, diazo, through sulfur dioxide, oxychloride, ammoniation ring, nitrogen methylation, carbonitriding, reduction, open-loop, a sulfonylation and condensation of the eleven step to make the methyl two sulphur are prosperous. The invention synthetic the methyl two sulphur are prosperous, the raw material is cheap, simple operation, mild condition, low equipment requirements, high yield, is suitable for industrial production, and the practicability is strong. (by machine translation)

A NEW CLASS OF MU-OPIOID RECEPTOR AGONISTS

The present invention provides a compound having the structure (I) or a pharmaceutically acceptable salt or ester thereof.

Tricyclic benzoylpyrazole derivatives used as a herbicide

Tricyclic benzoylpyrazole derivatives of the formula I wherein X, Y, R1, R2, R6, R7, R3, R4, R5, l, R8 and R9 are as defined in the disclosure and their agriculturally useful salts; processes and intermediates for preparing the tricyclic benzoylpyrazole derivatives; compositions comprising them and the use of these derivatives or of the compositions comprising them for controlling undesirable plants are described.

Facile synthesis of 1, 2-benzisothiazole-3-one-1,1-dioxide methylsulfonyl derivatives

An improved and general synthesis of saccharin methylthio and methylsulfone derivatives from chloro-substituted saccharins is presented. A large-scale procedure for preparation of chloro-substituted saccharins was developed. Treatment of the saccharin chlorides with sodium thiomethoxide and t-BuOK in DMF gave the saccharin methyl sulfides, which upon chromium(VI) oxide catalyzed oxidation with periodic acid afforded the corresponding saccharin methylsulfones in high yields.

Tricyclic benzoylcyclohexanedione derivatives

Tricyclic benzoylcyclohexanedione derivatives of the formula I where X, Y, R1, R2, R3, R4, R5, R9, and m are defined herein, and their agriculturally useful salts. Process for preparing the tricyclic benzoylcyclohexanedione derivatives; compositions comprising them and the use of these derivatives or of the compositions comprising them for controlling undesirable plants are described.

Endothelin receptor antagonists: Synthesis and structure-activity relationships of substituted benzothiazine-1,1-dioxides

The development of benzothiazine-1,1-dioxide derivatives as a new structural class of potent endothelin receptor antagonists is described. Structure-activity relationships (SAR) revealed that PD164800 (1) is a potent antagonist of the ET(A) receptor subtype. Copyright (C) 1998 Elsevier Science Ltd.