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Catalog Number:
41646
CAS Number:
161511-85-9
( S )-1-( tert -Butoxycarbonyl)-2-azétidineméthanol
Purity:
≥ 98 % (pureté chirale)
Synonym(s):
( S )-1-Boc-2-azétidineméthanol
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$116.67 /100 mg
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Product Information

(S)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure, featuring a tert-butoxycarbonyl group, enhances its stability and reactivity, making it an essential intermediate in the development of biologically active molecules. Researchers and industry professionals appreciate its role in the preparation of peptide-based drugs and other complex organic compounds. The compound's hydroxymethyl group also allows for further functionalization, expanding its application potential in medicinal chemistry and material science.

In addition to its pharmaceutical applications, (S)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol is valuable in the field of organic synthesis, where it serves as a building block for various chemical transformations. Its ability to undergo selective reactions makes it a preferred choice for chemists looking to streamline their synthesis processes. With its proven efficacy and adaptability, this compound stands out as a crucial tool for advancing research and development in multiple sectors.

Synonyms
( S )-1-Boc-2-azétidineméthanol
CAS Number
161511-85-9
Purity
≥ 98 % (pureté chirale)
Molecular Formula
C 9 H 17 NO 3
Molecular Weight
187.24
MDL Number
MFCD03093620
PubChem ID
14821739
Density
1,05 g/mL
Appearance
Liquide transparent incolore à jaune clair
Refractive Index
n20D 1.46
Optical Rotation
[a]20D = -76 à -72 ° (C = 1 dans MeOH)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
( S )-1-Boc-2-azétidineméthanol
CAS Number
161511-85-9
Purity
≥ 98 % (pureté chirale)
Molecular Formula
C 9 H 17 NO 3
Molecular Weight
187.24
MDL Number
MFCD03093620
PubChem ID
14821739
Density
1,05 g/mL
Appearance
Liquide transparent incolore à jaune clair
Refractive Index
n20D 1.46
Optical Rotation
[a]20D = -76 à -72 ° (C = 1 dans MeOH)
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of new drugs targeting neurological disorders.
  • Peptide Synthesis: It is employed in the synthesis of peptides, enhancing the stability and bioavailability of therapeutic agents, which is crucial for effective drug formulation.
  • Bioconjugation: The compound is useful in bioconjugation processes, allowing for the attachment of biomolecules to drugs, improving targeted delivery and efficacy.
  • Research in Organic Chemistry: It acts as a building block in organic synthesis, facilitating the creation of complex molecules, which is essential for advancing chemical research.
  • Material Science: This chemical is explored in the development of novel materials, particularly in creating polymers with specific properties for industrial applications.

Citations