Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
26466
CAS Number:
197892-14-1
S-2-(Boc-amino)-4-(Z-amino)-1-butanol
Purity:
≥ 99.9% (Chiral HPLC)
Synonym(s):
Boc-Dab(Z)-ol
Documents
$72.31 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(S)-2-(Boc-amino)-4-(Z-amino)-1-butanol is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound, known for its unique structure, serves as a valuable building block in the development of various bioactive molecules. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal candidate for peptide synthesis and other complex organic reactions. Researchers appreciate its role in the synthesis of amino acids and peptides, which are crucial for drug development and therapeutic applications.

In addition to its synthetic utility, (S)-2-(Boc-amino)-4-(Z-amino)-1-butanol has shown promise in the development of novel therapeutic agents, particularly in the area of cancer research and treatment. Its ability to facilitate the introduction of functional groups into larger molecular frameworks enhances its appeal for medicinal chemists looking to innovate in drug design. With its robust properties and practical applications, this compound stands out as a key resource for professionals in the pharmaceutical and chemical industries.

Synonyms
Boc-Dab(Z)-ol
CAS Number
197892-14-1
Purity
≥ 99.9% (Chiral HPLC)
Molecular Formula
C17H26N2O5
Molecular Weight
338.4
MDL Number
MFCD22381071
PubChem ID
10593105
Melting Point
84 - 89 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -28 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-Dab(Z)-ol
CAS Number
197892-14-1
Purity
≥ 99.9% (Chiral HPLC)
Molecular Formula
C17H26N2O5
Molecular Weight
338.4
MDL Number
MFCD22381071
PubChem ID
10593105
Melting Point
84 - 89 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -28 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-2-(Boc-amino)-4-(Z-amino)-1-butanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, facilitating the creation of complex structures for pharmaceuticals.
  • Drug Development: Its unique properties make it valuable in the development of new drugs, particularly in targeting specific biological pathways.
  • Biotechnology: Researchers use this chemical in various biotechnological applications, including the design of enzyme inhibitors and other bioactive molecules.
  • Medicinal Chemistry: It plays a crucial role in medicinal chemistry for optimizing lead compounds, enhancing their efficacy and selectivity.
  • Research on Amino Acid Derivatives: This compound is instrumental in studying amino acid derivatives, contributing to advancements in understanding protein interactions and functions.

Citations