METHYL THIOPHENE-3-ACETATE
- Name METHYL THIOPHENE-3-ACETATE
- CAS 58414-52-1
- Purity 99%
Product Details
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1.What is the METHYL THIOPHENE-3-ACETATE ?
Methyl thiophene-3-acetate, with the molecular formula C8H8O2S, is a colorless to pale yellow liquid chemical compound. It is characterized by a strong, sweet, and floral odor, and is known for its low toxicity, making it a relatively safe compound for intended uses. This versatile substance is commonly utilized in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of perfumes and fragrances due to its distinctive scent. Additionally, it serves as a flavoring agent in the food industry.
2.What is the CAS number for METHYL THIOPHENE-3-ACETATE ?
The CAS number of METHYL THIOPHENE-3-ACETATE is 58414-52-1.
3.What are another words for METHYL THIOPHENE-3-ACETATE ?
Synonyms?for?METHYL THIOPHENE-3-ACETATE 58414-52-1:2-(Thien-3-yl)aceticacid methyl ester; Methyl 3-thienylacetate; Methyl 3-thiopheneacetate
4.What is METHYL THIOPHENE-3-ACETATE (58414-52-1) used for?
Used in Pharmaceutical and Agrochemical Industries:
Methyl thiophene-3-acetate is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a valuable component in the development of new drugs and agricultural products, contributing to advancements in these fields.
Used in Perfume and Fragrance Industry:
Methyl thiophene-3-acetate is used as a fragrance ingredient for its strong, sweet, and floral scent. It adds depth and complexity to perfumes and other fragranced products, enhancing their appeal and longevity.
Used in Food Industry:
As a flavoring agent, methyl thiophene-3-acetate is incorporated into the food industry to impart specific tastes and aromas to various food products. Its use in this industry is regulated to ensure safety and quality standards are met.
InChI:InChI=1/C7H8O2S/c1-9-7(8)4-6-2-3-10-5-6/h2-3,5H,4H2,1H3
Relevant articles related to METHYL THIOPHENE-3-ACETATE:
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Article |
Source |
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Synthesis and characterization of poly(3-thiophene acetic acid)/Fe 3O4 nanocomposite |
Aydin,Durmus,Kavas,Esat,S?zeri,Baykal,Yilmaz,Toprak , p. 1120 - 1126 (2011) |
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Preparation and electrochemical performance of TEMPO-modified polyterthiophene electrode obtained by electropolymerization |
Niu, Pengfei,Cai, Yanchao,Guo, Ming,Shen, Zhenlu,Li, Meichao , (2020) |
|
syn-Selective Michael Reaction of α-Branched Aryl Acetaldehydes with Nitroolefins Promoted by Squaric Amino Acid Derived Bifunctional Br?nsted Bases |
Campano, Teresa E.,García-Urricelqui, Ane,Mielgo, Antonia,Palomo, Claudio,de Cózar, Abel supporting information, p. 3604 - 3612 (2021/07/26) |
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