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Catalog Number:
24345
CAS Number:
1009093-14-4
Boc-( 1R , 2R -(-)-2-amino-1-fenil-1,3-propanodiol
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-D- treo -3-fenilserinol
Documents
$242.56 /100 mg
Tamaño
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Product Information

Boc-(1R,2R)-(-)-2-amino-1-phenyl-1,3-propanediol is a versatile compound widely utilized in pharmaceutical research and development. This compound, also known as tert-butyl N-[(1R,2R)-1,3-dihydroxy-1-phenylpropan-2-yl]carbamate, serves as a crucial building block in the synthesis of various bioactive molecules. Its unique structure, featuring a Boc (tert-butoxycarbonyl) protecting group, enhances its stability and reactivity, making it an ideal candidate for peptide synthesis and medicinal chemistry applications.

Researchers appreciate its role in the development of potential therapeutic agents, particularly in the fields of neuropharmacology and oncology. The compound's ability to facilitate the introduction of amino and hydroxyl functionalities allows for the creation of diverse derivatives, which can be tailored for specific biological activities. With its favorable properties and applications, Boc-(1R,2R)-(-)-2-amino-1-phenyl-1,3-propanediol stands out as a valuable resource for professionals aiming to innovate in drug discovery and development.

Synonyms
Boc-D- treo -3-fenilserinol
CAS Number
1009093-14-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C14H21NO4
Molecular Weight
267.32
MDL Number
MFCD04974332
PubChem ID
18329302
Appearance
Jarabe de color amarillo pálido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-D- treo -3-fenilserinol
CAS Number
1009093-14-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C14H21NO4
Molecular Weight
267.32
MDL Number
MFCD04974332
PubChem ID
18329302
Appearance
Jarabe de color amarillo pálido
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-(1R,2R)-(-)-2-amino-1-phenyl-1,3-propanediol 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 and cardiovascular conditions.
  • Peptide Synthesis: It is employed as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure, enhancing the efficiency of drug design.
  • Biochemical Research: Researchers use this compound to study enzyme interactions and mechanisms, aiding in the understanding of biological processes and potential therapeutic targets.
  • Material Science: The compound is explored for its potential applications in creating novel materials with specific properties, such as improved biocompatibility for medical devices.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing chemists to produce specific enantiomers that are crucial in developing effective drugs with fewer side effects.

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