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Catalog Number:
25857
CAS Number:
474843-40-8
3-Amino-5-(4-(benzyloxy)phényl)thiophène-2-carboxylate de méthyle
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ester méthylique de l'acide 3-amino-5-(4-benzyloxyphényl)thiophène-2-carboxylique
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$120.88 /100 mg
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Product Information

Methyl 3-Amino-5-(4-(benzyloxy)phenyl)thiophene-2-carboxylate is a versatile compound with significant potential in pharmaceutical research and development. This compound features a unique thiophene structure, which enhances its reactivity and compatibility with various biological systems. Its amino and carboxylate functional groups make it an excellent candidate for further derivatization, allowing researchers to explore a wide range of applications, particularly in the synthesis of novel therapeutic agents.

In the pharmaceutical industry, Methyl 3-Amino-5-(4-(benzyloxy)phenyl)thiophene-2-carboxylate can be utilized in the development of anti-inflammatory and anticancer drugs, owing to its ability to interact with specific biological targets. Additionally, its benzyloxy group contributes to improved solubility and bioavailability, making it a valuable asset in drug formulation. Researchers and industry professionals can leverage this compound's unique properties to create innovative solutions that address unmet medical needs, enhancing the efficacy and safety of new therapeutic options.

Synonyms
Ester méthylique de l'acide 3-amino-5-(4-benzyloxyphényl)thiophène-2-carboxylique
CAS Number
474843-40-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 19 H 17 NON 3 S
Molecular Weight
339.41
MDL Number
MFCD04116403
PubChem ID
2756348
Melting Point
155-162 ?C
Appearance
Poudre cristalline jaune pâle
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester méthylique de l'acide 3-amino-5-(4-benzyloxyphényl)thiophène-2-carboxylique
CAS Number
474843-40-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 19 H 17 NON 3 S
Molecular Weight
339.41
MDL Number
MFCD04116403
PubChem ID
2756348
Melting Point
155-162 ?C
Appearance
Poudre cristalline 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

Methyl 3-Amino-5-(4-(benzyloxy)phenyl)thiophene-2-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of novel pharmaceuticals, particularly in creating targeted therapies for various diseases, including cancer.
  • Organic Electronics: Its unique electronic properties make it suitable for use in organic light-emitting diodes (OLEDs) and organic photovoltaic cells, enhancing energy efficiency in electronic devices.
  • Material Science: The compound is explored for its potential in developing advanced materials with specific thermal and mechanical properties, beneficial for industries like aerospace and automotive.
  • Biochemical Research: It is employed in studies investigating enzyme interactions and metabolic pathways, aiding researchers in understanding complex biological systems.
  • Agrochemicals: The compound is being examined for its efficacy in developing new agrochemical products that improve crop yield and resistance to pests, contributing to sustainable agriculture.

Citations