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Catalog Number:
11835
CAS Number:
259221-91-5
Boc-D-glutamic acid γ-allyl ester
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-Glu(OAll)-OH, Boc-D-glutamic acid 5-allyl ester
Documents
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Product Information

Boc-D-glutamic acid g-allyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This derivative of glutamic acid features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity in various chemical reactions. Its unique structure allows for selective modifications, making it an essential building block in the development of bioactive peptides and drug candidates. Researchers appreciate its ability to facilitate the introduction of functional groups, enabling the design of compounds with tailored properties for specific applications in medicinal chemistry.

In addition to its role in peptide synthesis, Boc-D-glutamic acid g-allyl ester is also employed in the production of advanced materials and as an intermediate in organic synthesis. Its compatibility with various coupling reactions and ease of handling make it a preferred choice for professionals in the pharmaceutical and biotechnology sectors. With its potential to streamline the synthesis of complex molecules, this compound stands out as a valuable asset for researchers aiming to innovate in drug development and related fields.

Synonyms
Boc-D-Glu(OAll)-OH, Boc-D-glutamic acid 5-allyl ester
CAS Number
259221-91-5
Purity
≥ 99% (HPLC)
Molecular Formula
C13H21NO6
Molecular Weight
287.4
MDL Number
MFCD01862283
PubChem ID
14779839
Melting Point
43-49 ºC
Appearance
White solid
Optical Rotation
[a]D20 = + 10 ± 2 º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Glu(OAll)-OH, Boc-D-glutamic acid 5-allyl ester
CAS Number
259221-91-5
Purity
≥ 99% (HPLC)
Molecular Formula
C13H21NO6
Molecular Weight
287.4
MDL Number
MFCD01862283
PubChem ID
14779839
Melting Point
43-49 ºC
Appearance
White solid
Optical Rotation
[a]D20 = + 10 ± 2 º (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-D-glutamic acid g-allyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of bioactive compounds and pharmaceuticals.
  • Drug Development: Its unique structure allows for modifications that enhance the solubility and bioavailability of drug candidates, making it valuable in medicinal chemistry.
  • Bioconjugation: The allyl group can be used for selective reactions, facilitating the attachment of biomolecules to surfaces or other compounds, which is crucial in creating targeted therapies.
  • Research in Neuroscience: This compound can be utilized in studies related to neurotransmitter functions, potentially leading to advancements in understanding neurological disorders.
  • Material Science: Its properties enable the development of novel materials with specific functionalities, such as hydrogels or coatings, which can be applied in various industrial sectors.

Citations