3133-78-6

Basic information

• Product Name: 3-Methylbenzothiophene-2-carboxylicacid
• Synonyms: 3-Methylbenzothiophene-2-carboxylicacid;Benzo[b]thiophene-2-carboxylic acid,3-methyl-
• CAS NO: 3133-78-6
• Molecular Formula: C₁₀H₈O₂S
• Molecular Weight: 192.23432
• Product Categories: Heterocycle-oher series
• Mol File: 3133-78-6.mol
• Article Data: 6

Chemical Properties

• Melting Point: 241-244°C
• Boiling Point: 379.9 °C at 760 mmHg
• Flash Point: 183.6 °C
• Appearance: /
• Density: 1.355 g/cm³
• Vapor Pressure: 1.9E-06mmHg at 25°C
• Storage Temp.: 2-8°C
• PKA: 3.23±0.30(Predicted)
• CAS DataBase Reference: 3-Methylbenzothiophene-2-carboxylicacid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Methylbenzothiophene-2-carboxylicacid(3133-78-6)
• EPA Substance Registry System: 3-Methylbenzothiophene-2-carboxylicacid(3133-78-6)

Safety Data

• Hazardous Substances Data: 3133-78-6(Hazardous Substances Data)

Usage

General Description

3-Methylbenzothiophene-2-carboxylic acid is a synthetic organic compound, classified as a member of the benzothiophenes, which are heterocyclic compounds containing a benzene fused to a thiophene ring. The molecular formula for this particular substance is C10H8O2S. It is derived from coal tar or petroleum processing. This specific chemical is not widely discussed in available literature, indicating that the compound is either nonessential or has not been thoroughly researched. The exact properties, reactions, safety hazards, or applications of 3-methylbenzothiophene-2-carboxylic acid have not been extensively documented. Like many chemicals, safe handling would be essential in a laboratory or industrial setting until more specific details about its properties are known.

InChI:InChI=1/C10H8O2S/c1-6-7-4-2-3-5-8(7)13-9(6)10(11)12/h2-5H,1H3,(H,11,12)/p-1

Upstream product

• 1455-18-1 3-methylbenzothiophene 
• 573722-35-7 benzo[b]thiophen-3-ylmethyl-magnesium chloride 
• 15719-64-9 methylammonium carbonate 
• 60-29-7 diethyl ether 
• 541-41-3 chloroformic acid ethyl ester 
• 3216-47-5 3-chloromethylbenzothiophene 
• 2142-68-9 1-(2-chlorophenyl)ethanone 
• 68-11-1 mercaptoacetic acid 
• 6314-28-9 benzo[b]thiophene-2-carboxylic acid 
• 75-24-1 trimethylaluminum 
• 3133-81-1 3-methylbenzo[b]thiophene-2-carboxylic acid methyl ester 
• 445-27-2 2'-Fluoroacetophenone 
• 124-38-9 carbon dioxide 
• 875257-99-1 (2-acetyl-phenylsulfanyl)-acetic acid 

Downstream Products

• 1455-18-1 3-methylbenzothiophene 
• 1258844-19-7 3,3'-dimethyl-2,2'-bibenzo[b]thiophene 
• 1263757-42-1 2-(2,4,6-trifluorophenyl)-3-methylbenzo[b]thiophene 
• 1263757-12-5 3-methyl-2-(pentafluorophenyl)benzo[b]thiophene 
• 1263757-46-5 (2,4-difluoro-3-(3-methylbenzo[b]thiophen-2-yl)phenyl)-(phenyl)methanone 
• 1263757-48-7 methyl 3,5-difluoro-4-(3-methylbenzo[b]thiophen-2-yl)benzoate 
• 3216-49-7 3-methylbenzothiophene-2-carbonitrile 
• 41280-76-6 3-methylbenzo[b]thiophene-2-carbonyl chloride 
• 50288-76-1 2-chloro-3-methylbenzothiophene 

Relevant articles and documents

Redox-Neutral Photocatalytic C?H Carboxylation of Arenes and Styrenes with CO2

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METHOD FOR PROMOTING PLANT GROWTH

The present invention provides a method for promoting plant growth, which comprises treating a plant with at least one compound selected from a group consisting of a compound represented by the following Formula (1): and an agriculturally acceptable salt thereof, provided that a method for promoting plant growth which comprises treating plants with a compound corresponding to any one of the following (1) to (5) and an agriculturally acceptable salt thereof is excluded: (1) 4-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, (2) 5-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, (3) 6-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, (4) 7-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, and (5) Benzo[b]thiophene-2-carboxylic acid.

Direct carboxylation of thiophenes and benzothiophenes with the aid of EtAlCl2

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