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Catalog Number:
15696
CAS Number:
500770-66-1
Acide boc-( S -3-amino-3-(2-thiényl)propionique)
Purity:
99 % (HPLC)
Synonym(s):
Boc-D-β-Ala-(2-thiényl)-OH, ( S -Boc-2-thiényl-β-phénylalanine
Documents
$72.31 /100 mg
Taille
99 % (HPLC)">
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Product Information

Boc-(S)-3-amino-3-(2-thienyl)propionic acid is a valuable compound widely utilized in the field of medicinal chemistry and peptide synthesis. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and facilitates its incorporation into peptide chains. Its unique structure, characterized by the presence of a thiophene ring, provides distinct properties that can be leveraged in the development of novel therapeutics. Researchers have found this compound particularly useful in the synthesis of bioactive peptides and as a building block in the design of inhibitors targeting various biological pathways.

The compound's ability to enhance solubility and improve the pharmacokinetic profiles of peptides makes it an attractive choice for pharmaceutical applications. Its specific stereochemistry and functional groups allow for tailored modifications, enabling the creation of compounds with optimized biological activity. Whether in drug discovery or academic research, Boc-(S)-3-amino-3-(2-thienyl)propionic acid stands out as a versatile tool for professionals aiming to innovate in peptide-based therapies.

Synonyms
Boc-D-β-Ala-(2-thiényl)-OH, ( S -Boc-2-thiényl-β-phénylalanine
CAS Number
500770-66-1
Purity
99 % (HPLC)
Molecular Formula
C 12 H 17 NON 4 S
Molecular Weight
271.33
MDL Number
MFCD03427912
PubChem ID
2764289
Melting Point
83-89 °C
Appearance
Poudre blanc cassé
Optical Rotation
[a] D 25 = -58 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-D-β-Ala-(2-thiényl)-OH, ( S -Boc-2-thiényl-β-phénylalanine
CAS Number
500770-66-1
Purity
99 % (HPLC)
Molecular Formula
C 12 H 17 NON 4 S
Molecular Weight
271.33
MDL Number
MFCD03427912
PubChem ID
2764289
Melting Point
83-89 °C
Appearance
Poudre blanc cassé
Optical Rotation
[a] D 25 = -58 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(S)-3-amino-3-(2-thienyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of bioactive peptides that can be used in pharmaceuticals.
  • Drug Development: Its unique structural properties make it valuable in the design of novel drugs targeting specific biological pathways, especially in the field of neuropharmacology.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted drug delivery systems and improving the efficacy of therapeutic agents.
  • Research in Neuroscience: It plays a role in studies related to neurotransmitter systems, helping researchers understand the mechanisms of action for various neurological disorders.
  • Analytical Chemistry: This chemical is utilized in analytical methods to assess the purity and concentration of compounds in research laboratories, ensuring high-quality results in experiments.

Citations