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Catalog Number:
15695
CAS Number:
500788-98-7
Boc-(R-3-amino-3-(2-thienyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-Ala-(2-thienyl)-OH, (R-Boc-2-thienyl-β-phenylalanine
Documents
$72.31 /100MG
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Product Information

Boc-(R)-3-amino-3-(2-thienyl)propionic acid is a valuable compound widely utilized in the field of pharmaceutical research and development. This amino acid derivative features a unique thienyl group, which enhances its potential as a building block in the synthesis of bioactive molecules. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, making it an ideal candidate for peptide synthesis and medicinal chemistry applications. Researchers appreciate its role in developing novel therapeutics, particularly in the areas of neuropharmacology and cancer treatment, where specific amino acid configurations can significantly influence biological activity.

In addition to its applications in drug development, Boc-(R)-3-amino-3-(2-thienyl)propionic acid serves as a versatile intermediate in organic synthesis. Its structural characteristics enable the creation of compounds with tailored properties, facilitating advancements in materials science and biotechnology. The compound's stability and reactivity make it a preferred choice for chemists seeking to explore new pathways in synthetic chemistry. With its unique features and practical applications, this compound stands out as a crucial tool for researchers aiming to innovate in their respective fields.

Synonyms
Boc-L-β-Ala-(2-thienyl)-OH, (R-Boc-2-thienyl-β-phenylalanine
CAS Number
500788-98-7
Purity
≥ 98% (HPLC)
Molecular Formula
C12H17NO4S
Molecular Weight
271.33
MDL Number
MFCD03427950
PubChem ID
2764289
Melting Point
81-87 °C
Appearance
White powder
Optical Rotation
[a]D25 = +58 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-Ala-(2-thienyl)-OH, (R-Boc-2-thienyl-β-phenylalanine
CAS Number
500788-98-7
Purity
≥ 98% (HPLC)
Molecular Formula
C12H17NO4S
Molecular Weight
271.33
MDL Number
MFCD03427950
PubChem ID
2764289
Melting Point
81-87 °C
Appearance
White powder
Optical Rotation
[a]D25 = +58 ± 2º (C=1 in EtOH)
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

Boc-(R)-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 those that require specific stereochemistry for biological activity. Its protective Boc group allows for selective reactions, making it easier to construct complex peptide sequences.
  • Drug Development: In pharmaceutical research, it is used to develop novel drug candidates, especially in the field of neuropharmacology. Its unique thiophene structure can enhance the binding affinity of compounds to target receptors.
  • Bioconjugation: The compound is employed in bioconjugation techniques, where it can be used to attach biomolecules to surfaces or other molecules, improving the efficacy of therapeutic agents in targeted drug delivery systems.
  • Research on Amino Acid Analogues: It is valuable in studies exploring amino acid analogues, helping researchers understand the role of structure in biological function, which can lead to the discovery of new metabolic pathways.
  • Material Science: The compound finds applications in the development of functional materials, where its unique properties can be harnessed to create polymers or coatings with specific functionalities, such as enhanced conductivity or biocompatibility.

Citations