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Catalog Number:
06215
CAS Number:
32595-59-8
DL-ॆ-(2-Thienyl)-serine
Purity:
≥ 98%
Synonym(s):
DL-Ser(2-Thi)-OH
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Product Information

DL-b-(2-Thienyl)-serine is a versatile amino acid derivative that has garnered attention in various fields, particularly in pharmaceutical and biochemical research. This compound, characterized by its unique thiophene ring structure, offers potential applications in the development of novel therapeutic agents. Its structural similarity to natural amino acids allows it to participate in biological processes, making it a valuable tool for researchers exploring enzyme inhibition and receptor interactions.

In addition to its role in drug discovery, DL-b-(2-Thienyl)-serine has been investigated for its potential in neuropharmacology, where it may contribute to the understanding of neurotransmitter systems. Its unique properties, such as enhanced solubility and stability compared to similar compounds, make it an attractive candidate for formulation in various delivery systems. Researchers and industry professionals can leverage this compound to explore innovative solutions in medicinal chemistry and beyond, paving the way for advancements in therapeutic strategies.

Synonyms
DL-Ser(2-Thi)-OH
CAS Number
32595-59-8
Purity
≥ 98%
Molecular Formula
C7H9NO3S
Molecular Weight
187.2
MDL Number
MFCD00067304
PubChem ID
98096
Melting Point
181 - 185 ºC
Appearance
White or off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
DL-Ser(2-Thi)-OH
CAS Number
32595-59-8
Purity
≥ 98%
Molecular Formula
C7H9NO3S
Molecular Weight
187.2
MDL Number
MFCD00067304
PubChem ID
98096
Melting Point
181 - 185 ºC
Appearance
White or off-white powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

DL-b-(2-Thienyl)-serine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is explored for its potential as a therapeutic agent in treating neurological disorders, offering a unique structure that may enhance drug efficacy.
  • Biochemical Research: It serves as a valuable tool in studying protein interactions and enzyme activities, helping researchers understand complex biological processes.
  • Agrochemical Applications: The compound is investigated for its role in developing environmentally friendly pesticides, contributing to sustainable agriculture practices.
  • Material Science: It is used in the synthesis of novel materials, particularly in creating polymers with enhanced properties, which can be beneficial in various industrial applications.
  • Flavor and Fragrance Industry: Due to its unique thiophene structure, it is studied for potential applications in flavoring and fragrance formulations, offering distinctive sensory profiles.

Citations