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Catalog Number:
44243
CAS Number:
67488-46-4
2,5-dihidrotiofeno-3-carboxilato de metilo
Purity:
≥ 95% (GC)
Synonym(s):
Éster metílico del ácido 2,5-dihidrotiofeno-3-carboxílico
Documents
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Tamaño
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Product Information

Methyl 2,5-dihydrothiophene-3-carboxylate is a versatile compound known for its unique thiophene structure, which imparts distinctive properties beneficial for various applications. This compound is recognized for its role in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to undergo various chemical transformations makes it a valuable intermediate in the synthesis of more complex molecules. Researchers appreciate its utility in the creation of biologically active compounds, as well as its potential in the formulation of specialty chemicals.

In addition to its synthetic applications, Methyl 2,5-dihydrothiophene-3-carboxylate is also explored for its potential in materials science, particularly in the development of conductive polymers and organic electronic devices. Its favorable reactivity and stability under various conditions make it an attractive option for researchers looking to innovate in these fields. With its multifaceted applications and the growing interest in thiophene derivatives, this compound holds significant promise for advancing both research and industrial processes.

Synonyms
Éster metílico del ácido 2,5-dihidrotiofeno-3-carboxílico
CAS Number
67488-46-4
Purity
≥ 95% (GC)
Molecular Formula
C6H8O2S
Molecular Weight
144.19
MDL Number
MFCD04038417
PubChem ID
11457755
Melting Point
34 - 38 °C
Appearance
Polvo de color blanco a naranja a verde en grumos
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éster metílico del ácido 2,5-dihidrotiofeno-3-carboxílico
CAS Number
67488-46-4
Purity
≥ 95% (GC)
Molecular Formula
C6H8O2S
Molecular Weight
144.19
MDL Number
MFCD04038417
PubChem ID
11457755
Melting Point
34 - 38 °C
Appearance
Polvo de color blanco a naranja a verde en grumos
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Methyl 2,5-dihydrothiophene-3-carboxylate is widely utilized in research focused on:

  • Flavor and Fragrance Industry: This compound is used as a flavoring agent due to its pleasant aroma, enhancing the sensory experience in food products and perfumes.
  • Pharmaceutical Development: It serves as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new medications with improved efficacy.
  • Agricultural Chemicals: The compound is explored for its potential in creating agrochemicals, such as pesticides and herbicides, that are effective yet environmentally friendly.
  • Material Science: It is used in the formulation of specialty polymers and coatings, providing enhanced properties like durability and resistance to environmental factors.
  • Research Applications: In academic and industrial research, it is employed as a reagent in organic synthesis, facilitating the creation of complex chemical structures.

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