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Catalog Number:
14123
CAS Number:
77171-41-6
Ácido Boc-(2 R ,3 R -3-amino-2-hidroxi-4-fenilbutírico
Purity:
≥ 99% (pureza quiral)
Synonym(s):
Boc-( 2R , 3R- Apns-OH
Documents
$86.23 /50 mg
Tamaño
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Product Information

Boc-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid is a versatile compound widely utilized in pharmaceutical and biochemical research. 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 drug development. Its unique structure allows for the exploration of various biological activities, particularly in the fields of neuropharmacology and medicinal chemistry. Researchers have leveraged this compound in the synthesis of bioactive peptides and as a building block for more complex molecules, showcasing its potential in developing therapeutic agents targeting neurological disorders.

In addition to its applications in drug discovery, Boc-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid serves as a valuable tool in the study of enzyme interactions and metabolic pathways. Its ability to mimic natural amino acids while providing distinct chemical properties makes it a preferred choice for scientists aiming to explore structure-activity relationships. The compound's favorable characteristics, including its ease of modification and compatibility with various synthetic methodologies, position it as a key player in advancing research in pharmaceuticals and biochemistry.

Synonyms
Boc-( 2R , 3R- Apns-OH
CAS Number
77171-41-6
Purity
≥ 99% (pureza quiral)
Molecular Formula
C 15 H 21 N º 5
Molecular Weight
295.34
MDL Number
MFCD00214254
PubChem ID
3420379
Melting Point
158-164 ?C
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-( 2R , 3R- Apns-OH
CAS Number
77171-41-6
Purity
≥ 99% (pureza quiral)
Molecular Formula
C 15 H 21 N º 5
Molecular Weight
295.34
MDL Number
MFCD00214254
PubChem ID
3420379
Melting Point
158-164 ?C
Appearance
Sólido blanco
Conditions
Conservar entre 0 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

Boc-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric 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, allowing researchers to create complex peptides with specific functionalities, enhancing drug design.
  • Biochemical Research: The compound is valuable in studying enzyme interactions and protein folding, providing insights into cellular mechanisms and potential therapeutic targets.
  • Cosmetic Formulations: Its properties make it suitable for use in skin care products, where it can help in formulating compounds that promote skin hydration and elasticity.
  • Food Industry: The compound can be explored as a food additive for enhancing flavor profiles or as a nutritional supplement, contributing to health-focused food products.

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