215648-56-9

Basic information

• Product Name: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER
• Synonyms: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER
• CAS NO: 215648-56-9
• Molecular Formula: C₉H₉ClO₅S
• Molecular Weight: 264.68
• Mol File: 215648-56-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 394.0±32.0 °C(Predicted)
• Appearance: /
• Density: 1.407±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER(215648-56-9)
• EPA Substance Registry System: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER(215648-56-9)

Safety Data

• Hazardous Substances Data: 215648-56-9(Hazardous Substances Data)

Usage

General Description

2-(Chlorosulfonyl)-3-methoxybenzoic acid methyl ester is a chemical compound with the formula C9H9ClO5S. It is a methyl ester of 2-(chlorosulfonyl)-3-methoxybenzoic acid and is often used as an intermediate in the production of pharmaceuticals and agrochemicals. 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER is a white to light brown solid that is soluble in organic solvents such as methanol and acetone. It is typically used in chemical reactions for the synthesis of other compounds and is known for its strong and reactive chlorosulfonyl group, making it useful in various chemical transformations. Additionally, 2-(Chlorosulfonyl)-3-methoxybenzoic acid methyl ester is known to have a variety of potential applications in research and industry due to its versatile reactivity and usefulness as a building block in organic synthesis.

Upstream product

• 215648-27-4 2-mercapto-3-methoxybenzoic acid methyl ester 
• 157187-05-8 2-dimethylthiocarbamoyloxy-3-methoxybenzoic acid methyl ester 
• 157187-06-9 2-dimethylcarbamoylsulfanyl-3-methoxybenzoic acid methyl ester 
• 6342-70-7 3-methoxymethylsalicylate 
• 877-22-5 3-methoxysalicylic acid 

Relevant articles and documents

Substituted sulphonylamino(thio)carbonyl compounds as herbicides

The invention relates to novel substituted sulphonylamino(thio)carbonyl compounds of the formula (I) in whichA represents oxygen, sulphur, NH, N-alkyl, N-aryl, —CH=N—, or —N=CH—or —CH=CH—,Q represents oxygen or sulphur,R1 represents respectively optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl,R2 represents cyano, nitro, halogen or represents respectively optionally substituted alkyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulphinyl, alkylsulphonyl, alkenyl, alkinyl, alkenyloxy or alkinyloxy, andR3 represents respectively optionally substituted heterocyclyl having 5 ring members of which at least one represents oxygen, sulphur or nitrogen and a further one to three may represent nitrogen,(except for certain individual prior art compounds), furthermore to salts of novel compounds of the formula (I), to various processes and novel intermediates for preparing the novel compounds and to their use as herbicides.

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.