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Catalog Number:
12787
CAS Number:
218943-30-7
Boc-L-β-homoglutamic acid 6-benzyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-HomoGlu(OBzl)-OH, (S-3-(Boc-amino)adipic acid 6-benzyl ester
Documents
$141.41 /250MG
Pack Size Availability Price
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Product Information

Boc-L-b-homoglutamic acid 6-benzyl ester is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal building block for the development of complex peptides and pharmaceuticals. Its unique structure allows for selective reactions, facilitating the synthesis of bioactive compounds that can be used in drug discovery and development.

Researchers appreciate the compound's ability to serve as a precursor in the synthesis of various peptide sequences, particularly those that require specific functional groups for biological activity. Additionally, the benzyl ester moiety contributes to its lipophilicity, improving membrane permeability, which is crucial for therapeutic applications. With its robust profile, Boc-L-b-homoglutamic acid 6-benzyl ester stands out as a valuable tool for chemists and biochemists aiming to innovate in drug formulation and peptide-based therapies.

Synonyms
Boc-L-β-HomoGlu(OBzl)-OH, (S-3-(Boc-amino)adipic acid 6-benzyl ester
CAS Number
218943-30-7
Purity
≥ 98% (HPLC)
Molecular Formula
C18H25NO6
Molecular Weight
351.4
MDL Number
MFCD01862936
PubChem ID
4393169
Appearance
White powder
Optical Rotation
[a]D25 = -8.5 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-β-HomoGlu(OBzl)-OH, (S-3-(Boc-amino)adipic acid 6-benzyl ester
CAS Number
218943-30-7
Purity
≥ 98% (HPLC)
Molecular Formula
C18H25NO6
Molecular Weight
351.4
MDL Number
MFCD01862936
PubChem ID
4393169
Appearance
White powder
Optical Rotation
[a]D25 = -8.5 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-L-b-homoglutamic acid 6-benzyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: It plays a role in creating drug candidates that target specific biological pathways. Researchers leverage its unique structure to design molecules with improved efficacy and reduced side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to biomolecules for targeted delivery systems. This application is crucial in developing therapies that require precise targeting of cells or tissues.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research to understand neurotransmitter functions and develop potential treatments for neurological disorders.
  • Material Science: The compound is also investigated for its potential in creating novel materials with specific properties, such as enhanced biocompatibility for medical devices.

Citations