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Catalog Number:
25855
CAS Number:
91076-94-7
3-Amino-5-(4-chlorophényl)thiophène-2-carboxylate d'éthyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 3-amino-5-(4-chlorophényl)-thiophène-2-carboxylique
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$58.39 /250 mg
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Product Information

Ethyl 3-Amino-5-(4-chlorophenyl)thiophene-2-carboxylate is a versatile compound with significant applications in pharmaceutical research and development. This compound features a unique thiophene ring structure, which enhances its potential as a building block in the synthesis of various bioactive molecules. Its amino and carboxylate functional groups contribute to its reactivity, making it an ideal candidate for the development of novel therapeutic agents, particularly in the fields of anti-inflammatory and antimicrobial research.

Researchers have utilized Ethyl 3-Amino-5-(4-chlorophenyl)thiophene-2-carboxylate in the synthesis of targeted drug compounds, benefiting from its ability to undergo various chemical transformations. Its chlorophenyl substituent further enhances its biological activity, allowing for the exploration of new pharmacological properties. This compound stands out for its potential to streamline the drug discovery process, offering a reliable and efficient pathway for the development of innovative treatments.

Synonyms
Ester éthylique de l'acide 3-amino-5-(4-chlorophényl)-thiophène-2-carboxylique
CAS Number
91076-94-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H12ClNO2S
Molecular Weight
281.76
MDL Number
MFCD06336766
PubChem ID
2118786
Melting Point
105-113 ?C
Appearance
Poudre amorphe jaune pâle
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester éthylique de l'acide 3-amino-5-(4-chlorophényl)-thiophène-2-carboxylique
CAS Number
91076-94-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H12ClNO2S
Molecular Weight
281.76
MDL Number
MFCD06336766
PubChem ID
2118786
Melting Point
105-113 ?C
Appearance
Poudre amorphe jaune pâle
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl 3-Amino-5-(4-chlorophenyl)thiophene-2-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders, enhancing drug efficacy.
  • Agricultural Chemistry: It is used in developing agrochemicals, providing effective solutions for pest control while minimizing environmental impact compared to traditional pesticides.
  • Material Science: The compound is explored for its potential in creating advanced materials, such as conductive polymers, which are essential for electronic applications.
  • Biochemical Research: It is employed in studies investigating enzyme interactions and metabolic pathways, aiding researchers in understanding complex biological systems.
  • Analytical Chemistry: This chemical is utilized in developing analytical methods for detecting and quantifying thiophene derivatives, offering high sensitivity and specificity in various samples.

Citations