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Catalog Number:
12960
CAS Number:
75937-12-1
6-(boc-amino)-1-hexanol
Purity:
≥ 95 % (RMN)
Synonym(s):
tert -butyle N- (6-hydroxyhexyle)carbamate, 6-Boc-Acp-ol
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Product Information

Liaison; préparation de l'iodure

Synonyms
tert -butyle N- (6-hydroxyhexyle)carbamate, 6-Boc-Acp-ol
CAS Number
75937-12-1
Purity
≥ 95 % (RMN)
Molecular Formula
C 11 H 23 NO 3
Molecular Weight
217.31
MDL Number
MFCD01862954
PubChem ID
4146612
Melting Point
37-41 ?C
Appearance
Solide blanc
Conditions
Conserver à 0-8 °C
General Information
Synonyms
tert -butyle N- (6-hydroxyhexyle)carbamate, 6-Boc-Acp-ol
CAS Number
75937-12-1
Purity
≥ 95 % (RMN)
Molecular Formula
C 11 H 23 NO 3
Molecular Weight
217.31
MDL Number
MFCD01862954
PubChem ID
4146612
Melting Point
37-41 ?C
Appearance
Solide blanc
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

6-(Boc-amino)-1-hexanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure.
  • Drug Development: It is used in the formulation of drug candidates, particularly in enhancing solubility and bioavailability, which is crucial for effective therapeutic applications.
  • Bioconjugation: The compound plays a significant role in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the efficacy of drug delivery systems.
  • Polymer Chemistry: It is applied in the development of functional polymers, contributing to materials with tailored properties for applications in coatings and adhesives.
  • Research in Biochemistry: This chemical aids in studying enzyme interactions and protein folding, providing insights that are essential for understanding biological processes.

Citations