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Catalog Number:
01381
CAS Number:
58521-49-6
Boc-(3S,4S-4-amino-3-hydroxy-6-methylheptanoic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-Sta(3S,4S-OH, (3S,4S-4-(Boc-amino)-3-hydroxy-6-methylheptanoicacid
Documents
$134.70 /100MG
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Product Information

Boc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid is a versatile amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers focused on synthesizing complex peptides and biologically active molecules. Its unique structure, characterized by a hydroxyl and amino group, allows for diverse modifications, facilitating the development of novel therapeutics and bioactive compounds.

In the field of medicinal chemistry, Boc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid is utilized in the design of peptide-based drugs, particularly those targeting specific biological pathways. Its application extends to the synthesis of cyclic peptides and other derivatives, which are crucial in drug discovery and development. Researchers appreciate its compatibility with various coupling reagents and reaction conditions, making it a valuable building block in the synthesis of tailored compounds for therapeutic applications.

Synonyms
Boc-Sta(3S,4S-OH, (3S,4S-4-(Boc-amino)-3-hydroxy-6-methylheptanoicacid
CAS Number
58521-49-6
Purity
≥ 98% (HPLC)
Molecular Formula
C13H25NO5
Molecular Weight
275.36
MDL Number
MFCD00063180
Appearance
Amorphous white powder
Optical Rotation
[a]D = -42.5 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-Sta(3S,4S-OH, (3S,4S-4-(Boc-amino)-3-hydroxy-6-methylheptanoicacid
CAS Number
58521-49-6
Purity
≥ 98% (HPLC)
Molecular Formula
C13H25NO5
Molecular Weight
275.36
MDL Number
MFCD00063180
Appearance
Amorphous white powder
Optical Rotation
[a]D = -42.5 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing the efficiency of the process.
  • Drug Development: It is used in the development of pharmaceutical compounds, particularly in creating novel therapeutics that target specific biological pathways.
  • Biotechnology: The compound plays a role in the production of biologically active molecules, aiding in the engineering of proteins and enzymes for various applications.
  • Research in Neuroscience: It is involved in studies related to neurotransmitter systems, contributing to the understanding of neurological disorders and potential treatments.
  • Cosmetic Formulations: The compound is explored for its potential in skincare products due to its amino acid properties, which may enhance skin health and hydration.

Citations