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Catalog Number:
16635
CAS Number:
119768-44-4
Boc-( R -1-amino-2-propanol
Purity:
≥ 99 % (dosage, pureté chirale)
Synonym(s):
N -Boc-( R -isopropanolamine, tert -butyle ( R -2-hydroxy-1-propylcarbamate
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Product Information

Boc-(R)-1-amino-2-propanol is a versatile compound widely utilized in the synthesis of pharmaceuticals and fine chemicals. This chiral amino alcohol serves as a crucial building block in the development of various bioactive molecules, particularly in the production of peptide-based drugs. Its unique tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, making it an ideal choice for complex organic synthesis. Researchers appreciate its ability to enhance the solubility and stability of intermediates during chemical reactions, which can lead to improved yields and purities in final products.

In addition to its applications in medicinal chemistry, Boc-(R)-1-amino-2-propanol is also employed in the formulation of agrochemicals and specialty chemicals. Its chiral nature provides an advantage in the creation of enantiomerically pure compounds, which are essential in the pharmaceutical industry for ensuring efficacy and safety. The compound's favorable properties and broad applicability make it a valuable asset for researchers and industry professionals seeking reliable and efficient solutions in their chemical processes.

Synonyms
N -Boc-( R -isopropanolamine, tert -butyle ( R -2-hydroxy-1-propylcarbamate
CAS Number
119768-44-4
Purity
≥ 99 % (dosage, pureté chirale)
Molecular Formula
C 8 H 17 NO 3
Molecular Weight
175.23
MDL Number
MFCD04974338
PubChem ID
9920508
Appearance
Liquide clair et incolore
Boiling Point
95-100 °C/1,2 mmHg
Conditions
Conserver à 0-8 °C
General Information
Synonyms
N -Boc-( R -isopropanolamine, tert -butyle ( R -2-hydroxy-1-propylcarbamate
CAS Number
119768-44-4
Purity
≥ 99 % (dosage, pureté chirale)
Molecular Formula
C 8 H 17 NO 3
Molecular Weight
175.23
MDL Number
MFCD04974338
PubChem ID
9920508
Appearance
Liquide clair et incolore
Boiling Point
95-100 °C/1,2 mmHg
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(R)-1-amino-2-propanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for amino acids during peptide synthesis, enhancing the efficiency and selectivity of reactions.
  • Drug Development: It is used in the development of pharmaceuticals, particularly in creating compounds that require specific stereochemistry for biological activity.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutics.
  • Material Science: It finds applications in the formulation of polymers and materials, improving properties such as solubility and stability in various environments.
  • Research in Chiral Catalysis: The compound is employed in studies involving chiral catalysts, aiding in the development of more efficient and environmentally friendly synthetic pathways.

Citations