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Catalog Number:
33442
CAS Number:
145432-51-5
( 2S , 3R- Boc-β-metil-L-Phe-OH
Purity:
≥ 97 % (HPLC)
Synonym(s):
(2 S ,3 R - N -Boc-2-Amino-3-fenilbutirilácido
Documents
$247.77 /5 mg
Tamaño
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Product Information

The compound (2S,3R)-Boc-b-methyl-L-Phe-OH, also known as Boc-b-methyl-L-phenylalanine, is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. Its unique structure, featuring a tert-butoxycarbonyl (Boc) protecting group, allows for selective reactions, making it an essential building block in the development of bioactive peptides and therapeutic agents. Researchers appreciate its stability and ease of handling, which facilitate the synthesis of complex molecules with high purity and yield.

This compound is particularly relevant in the fields of medicinal chemistry and biochemistry, where it serves as a precursor for the synthesis of peptide-based drugs and biologically active compounds. Its applications extend to the development of targeted therapies and drug delivery systems, showcasing its potential in advancing pharmaceutical innovations. The ability to modify the Boc group further enhances its versatility, allowing for tailored modifications to meet specific research needs. With its robust profile, (2S,3R)-Boc-b-methyl-L-Phe-OH stands out as a crucial component in the toolkit of researchers and industry professionals alike.

Synonyms
(2 S ,3 R - N -Boc-2-Amino-3-fenilbutirilácido
CAS Number
145432-51-5
Purity
≥ 97 % (HPLC)
Molecular Formula
C15H21Nº4
Molecular Weight
279.33
MDL Number
MFCD02259713
PubChem ID
5152353
Appearance
Polvo blanco
Optical Rotation
[a] 20 D = 18,6 ± 1,8 º (C=1 en CHCl 3 )
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
(2 S ,3 R - N -Boc-2-Amino-3-fenilbutirilácido
CAS Number
145432-51-5
Purity
≥ 97 % (HPLC)
Molecular Formula
C15H21Nº4
Molecular Weight
279.33
MDL Number
MFCD02259713
PubChem ID
5152353
Appearance
Polvo blanco
Optical Rotation
[a] 20 D = 18,6 ± 1,8 º (C=1 en CHCl 3 )
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S,3R)-Boc-b-methyl-L-Phe-OH 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 pharmaceutical industry, where it helps create therapeutic proteins and hormones.
  • Drug Development: It plays a significant role in developing new drugs, especially in designing compounds that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Biotechnology: In biotechnology, it is used for modifying proteins to improve their stability and activity, which is crucial for creating more effective biopharmaceuticals.
  • Research in Neuroscience: This compound is utilized in studies related to neurotransmitter functions, aiding researchers in understanding brain chemistry and developing treatments for neurological disorders.
  • Cosmetic Formulations: Its properties make it suitable for use in cosmetic products, where it can enhance skin penetration and improve the delivery of active ingredients.

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