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

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

Uses

Used in Food and Beverage Industry:
Methyl 3-methoxythiophene-2-carboxylate is used as a flavoring agent for its sweet, floral, and fruity aroma, enhancing the taste and scent of various food and beverage products.
Used in Cosmetic Industry:
In the cosmetic industry, Methyl 3-methoxythiophene-2-carboxylate is used as a fragrance ingredient, adding a pleasant and fruity scent to products, thereby improving consumer appeal.
Used in Pharmaceutical Industry:
Methyl 3-methoxythiophene-2-carboxylate is utilized in pharmaceutical applications due to its unique chemical properties, which may contribute to the development of new drugs or medicinal compounds.
Used in Agrochemical Industry:
Methyl 3-methoxythiophene-2-carboxylate also finds potential use in agrochemicals, where its chemical properties could be leveraged for the creation of novel agricultural products or enhancements to existing ones.

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 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 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.

NOVEL SPIROPIPERIDINE COMPOUNDS

A compound of the formula: or a pharmaceutically acceptable salt thereof as well as a pharmaceutical composition, and a method for treating diabetes.

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.

Shape selective recognition of T·A base pairs by hairpin polyamides containing N-terminal 3-methoxy (and 3-Chloro) thiophene residues

Hairpin polyamides selectively recognize predetermined DNA sequences with affinities comparable to naturally occurring proteins. Internal side-by-side pairs of unsymmetrical aromatic rings within the minor groove of DNA distinguish each of the four Watson-Crick base pairs. In contrast, N-terminal ring pairs exhibit less specificity, with the exception of Im/Py targeting G·C base pairs. In an effort to explore the sequence specificity of new ring pairs, a series of hairpin polyamides containing 3-substituted-thiophene-2-carboxamide residues at the N-terminus was synthesized. An N-terminal 3-methoxy (or 3-chloro) thiophene residue paired opposite Py displayed 6- (and 3-) fold selectivity for T·A relative to A·T base pair, while disfavoring G,C base pairs by >200-fold. Our data suggests shape selective recognition with projection of the 3-thiophene substituent (methoxy or chloro) to the floor of the minor groove.

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.