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Catalog Number:
15683
CAS Number:
499995-84-5
Acide boc-( S -3-amino-3-(3,4-diméthoxyphényl)propionique)
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-β-Phe(3,4-diméthoxy)-OH, ( S -Boc-3,4-Diméthoxy-β-phénylalanine
Documents
$72.31 /100 mg
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Product Information

Boc-(S)-3-amino-3-(3,4-dimethoxyphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and medicinal chemistry applications. Its unique structure, characterized by the presence of a 3,4-dimethoxyphenyl group, allows for significant interactions in biological systems, potentially leading to the development of novel therapeutic agents.

Researchers and industry professionals can leverage this compound in the synthesis of bioactive peptides and as a building block for drug discovery. Its ability to facilitate the introduction of amino acids into complex molecular frameworks positions it as a valuable tool in the design of targeted therapies. Additionally, the compound's favorable properties, including its stability and ease of handling, make it a preferred choice for laboratories focused on innovative drug development.

Synonyms
Boc-L-β-Phe(3,4-diméthoxy)-OH, ( S -Boc-3,4-Diméthoxy-β-phénylalanine
CAS Number
499995-84-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 16 H 236
Molecular Weight
325.36
MDL Number
MFCD03427907
PubChem ID
2764293
Melting Point
142-148 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -48 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(3,4-diméthoxy)-OH, ( S -Boc-3,4-Diméthoxy-β-phénylalanine
CAS Number
499995-84-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 16 H 236
Molecular Weight
325.36
MDL Number
MFCD03427907
PubChem ID
2764293
Melting Point
142-148 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -48 ± 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-(3,4-dimethoxyphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, providing a protective group that enhances the stability and yield of peptide chains.
  • Biochemical Research: Researchers utilize this compound to study protein interactions and enzyme activities, aiding in the understanding of biochemical pathways.
  • Material Science: The compound is explored for its potential in creating novel materials with specific properties, such as enhanced thermal stability and mechanical strength.
  • Drug Delivery Systems: Its unique structure allows for the development of advanced drug delivery systems, improving the bioavailability and targeted delivery of therapeutic agents.

Citations