62353-75-7

Basic information

• Product Name: METHYL 3-METHOXYTHIOPHENE-2-CARBOXYLATE
• Synonyms: METHYL 3-METHOXY-2-THIOPHENECARBOXYLATE;METHYL 3-METHOXYTHIOPHENE-2-CARBOXYLATE;3-METHOXYTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER;AKOS 92427;2-Methoxythiophene-2-carboxylic acid methylester;3-Methoxy-2-thiophenecarboxylic acid met;3-Methoxy-2-thiophenecarboxylic acid methyl ester
• CAS NO: 62353-75-7
• Molecular Formula: C₇H₈O₃S
• Molecular Weight: 172.2
• Product Categories: Esters;Thiophenes & Benzothiophenes;Thiophenes & Benzothiophenes
• Mol File: 62353-75-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 60-63°C
• Boiling Point: 255.3 °C at 760 mmHg
• Flash Point: 108.2 °C
• Appearance: /
• Density: 1.222 g/cm³
• Vapor Pressure: 0.0164mmHg at 25°C
• Refractive Index: 1.524
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL 3-METHOXYTHIOPHENE-2-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-METHOXYTHIOPHENE-2-CARBOXYLATE(62353-75-7)
• EPA Substance Registry System: METHYL 3-METHOXYTHIOPHENE-2-CARBOXYLATE(62353-75-7)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 62353-75-7(Hazardous Substances Data)

Usage

General Description

Methyl 3-methoxythiophene-2-carboxylate is an organic compound with the molecular formula C8H8O3S. It is a colorless liquid with a fruity odor and is commonly used as a flavor and fragrance ingredient in the food and cosmetic industry. This chemical is derived from the reaction of 3-methoxythiophene and methyl chloroformate and is commonly used in the production of various food and beverage products and perfumes. It is known for its sweet, floral, and fruity aroma and is often used in small concentrations to enhance the overall scent and flavor of the end product. Additionally, this compound has potential uses in pharmaceuticals and agrochemicals due to its unique chemical properties.

InChI:InChI=1/C7H8O3S/c1-9-5-3-4-11-6(5)7(8)10-2/h3-4H,1-2H3

Upstream product

• 5118-06-9 methyl 3-hydroxy-2-thiophenecarboxylate 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 
• 5118-07-0 3-hydroxythiophene-2-carboxylic acid 

Downstream Products

• 60166-83-8 3-methoxythiophene-2-carboxylic acid 
• 1372697-77-2 4-methoxy-2-(4-nitrophenyl)-thiophene 
• 1372697-48-7 methyl 3-methoxy-5-(4-nitrophenyl)-thiophene-2-carboxylate 
• 1372697-45-4 methyl 5-(4-formylphenyl)-3-methoxythiophene-2-carboxylate 
• 1372697-52-3 methyl 5-(2-cyanophenyl)-3-methoxythiophene-2-carboxylate 
• 1372697-50-1 methyl 5-(3-cyanophenyl)-3-methoxythiophene-2-carboxylate 
• 1309435-90-2 ethyl 3-[2-fluoro-4-[(5-formyl-4-methoxy-2-thienyl)methoxy]phenyl]propanoate 
• 1309435-89-9 ethyl 3-[2-fluoro-4-[[5-(hydroxymethyl)-4-methoxy-2-thienyl]methoxy]phenyl]propanoate 
• 1309435-88-8 ethyl 3-[4-[[5-[(teRt-butyl(dimethyl)silyl)oxymethyl]-4-methoxy-2-thienyl]methoxy]-2-fluoro-phenyl]propanoate 
• 1309436-41-6 ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate 
• 78031-17-1 3-methoxythiophene-2-carboxamide 
• 54450-14-5 3-methoxy-2-thenoyl chloride 

Relevant articles and documents

BORON CONTAINING COMPOUNDS AND THEIR USES

The present disclosure contemplates a boron-containing compound, a composition containing a pesticidal effective amount of that compound dissolved or dispersed in a carrier medium, and a method of reducing, ameliorating, or controlling an infestation by a pest, particularly a fungus, by administering a contemplated composition to a plant or animal in need.

DNA-BINDING POLYMERS

Methods and compositions are provided for forming complexes between dsDNA and novel DNA-binding polymers comprising N-terminal thiophene-containing moieties which exhibit selectivity for T-A base pairs. By appropriate choice of target sequences and DNA-binding polymers, complexes comprising polymer-DNA are obtained with high association constants. The formation of complexes can be used for identification of specific dsDNA sequences, for inhibiting gene transcription, and as a therapeutic for inhibiting proliferation of undesired cells or modulation of expression of specific genes.

Synthesis and antitumour activity of new derivatives of flavone-8- acetic acid (FAA). Part 31): 2-Heteroaryl derivatives

A range of 14 derivatives of flavone-8-acetic acid (FAA) with a heterocyclic substituent in place of the 2-phenyl group have been prepared and their anti-tumour activity evaluated in vitro against a panel of human and murine tumour cell lines and in vivo against MAC 15A. Some of the compounds, notably 2c,d and s, showed significant in vivo activity and these require further studies in order to evaluate their potential for development.