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Catalog Number:
15671
CAS Number:
499995-82-3
Boc-(S-3-amino-3-(2,3-dichlorophenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-β-Phe(2,3-DiCl)-OH, (S-Boc-2,3-dichloro-β-phenylalanine
Documents
$72.31 /250MG
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Product Information

Boc-(S)-3-amino-3-(2,3-dichlorophenyl)propionic acid is a valuable 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 allows for the exploration of various biological activities, particularly in the development of novel therapeutic agents targeting specific pathways in diseases.

Researchers have leveraged Boc-(S)-3-amino-3-(2,3-dichlorophenyl)propionic acid in the synthesis of bioactive compounds, contributing to advancements in drug discovery. Its ability to serve as a building block in complex organic synthesis highlights its importance in creating compounds with potential anti-inflammatory and analgesic properties. The compound's distinct dichlorophenyl moiety may also provide insights into structure-activity relationships, facilitating the design of more effective pharmaceuticals. With its practical applications and relevance in cutting-edge research, this compound stands out as a key resource for professionals in the chemical and pharmaceutical industries.

Synonyms
Boc-L-β-Phe(2,3-DiCl)-OH, (S-Boc-2,3-dichloro-β-phenylalanine
CAS Number
499995-82-3
Purity
≥ 99% (HPLC)
Molecular Formula
C14H17Cl2NO4
Molecular Weight
334.2
MDL Number
MFCD03427905
PubChem ID
2756791
Melting Point
146-152 °C
Appearance
White powder
Optical Rotation
[a]D25 = +24 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(2,3-DiCl)-OH, (S-Boc-2,3-dichloro-β-phenylalanine
CAS Number
499995-82-3
Purity
≥ 99% (HPLC)
Molecular Formula
C14H17Cl2NO4
Molecular Weight
334.2
MDL Number
MFCD03427905
PubChem ID
2756791
Melting Point
146-152 °C
Appearance
White powder
Optical Rotation
[a]D25 = +24 ± 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-(S)-3-amino-3-(2,3-dichlorophenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important building block in the synthesis of various pharmaceuticals, particularly in developing drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, allowing researchers to create complex peptides with specific biological activities, enhancing drug design.
  • Biochemical Research: The compound is valuable in studying enzyme interactions and protein functions, aiding researchers in understanding cellular mechanisms and disease pathways.
  • Material Science: It can be incorporated into polymer matrices to develop advanced materials with tailored properties, useful in coatings and biomedical applications.
  • Analytical Chemistry: This chemical is utilized as a standard in various analytical techniques, helping to ensure accuracy and reliability in chemical analysis.

Citations