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Catalog Number:
07441
CAS Number:
16338-48-0
H-Alil-L-glicina
Purity:
≥ 99,5 % (HPLC)
Synonym(s):
L-Gly(alil)-OH, Ácido ( S )-2-amino-4-pentenoico, H-Gly(alil)-OH
Documents
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Tamaño
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Product Information

H-Allyl-L-glycine is a versatile amino acid derivative known for its unique structural properties and functional applications in various fields. This compound, characterized by its allyl group, exhibits significant potential in the synthesis of peptides and as a building block in medicinal chemistry. Researchers have utilized H-Allyl-L-glycine in the development of novel pharmaceuticals, particularly in the design of compounds that target specific biological pathways. Its ability to enhance solubility and stability makes it an attractive choice for drug formulation, especially in the development of targeted therapies.

In addition to its pharmaceutical applications, H-Allyl-L-glycine is also employed in the field of biochemistry for the synthesis of bioactive compounds and as a chiral auxiliary in asymmetric synthesis. Its unique properties allow for improved reaction selectivity, making it a valuable tool for chemists aiming to create complex molecules with precision. The compound's compatibility with various reaction conditions further enhances its utility in research and industrial applications, positioning it as a key ingredient in the advancement of chemical synthesis and drug discovery.

Synonyms
L-Gly(alil)-OH, Ácido ( S )-2-amino-4-pentenoico, H-Gly(alil)-OH
CAS Number
16338-48-0
Purity
≥ 99,5 % (HPLC)
Molecular Formula
C5H9NO2
Molecular Weight
115.14
MDL Number
MFCD00002627
PubChem ID
14044
Appearance
Polvo o sólido de color blanco a blanquecino.
Optical Rotation
[a] D 20 = -37 ± 2 ° (C=1 en H 2 O)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
L-Gly(alil)-OH, Ácido ( S )-2-amino-4-pentenoico, H-Gly(alil)-OH
CAS Number
16338-48-0
Purity
≥ 99,5 % (HPLC)
Molecular Formula
C5H9NO2
Molecular Weight
115.14
MDL Number
MFCD00002627
PubChem ID
14044
Appearance
Polvo o sólido de color blanco a blanquecino.
Optical Rotation
[a] D 20 = -37 ± 2 ° (C=1 en H 2 O)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

H-Allyl-L-glycine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological and metabolic disorders.
  • Peptide Synthesis: It is employed in the formation of peptides, enhancing the structural diversity of peptides used in therapeutic applications, which can lead to more effective treatments.
  • Biochemical Research: Researchers use H-Allyl-L-glycine to study enzyme activity and protein interactions, providing insights into biochemical pathways and potential drug targets.
  • Food Industry: Its unique properties allow for applications in flavor enhancement and preservation, making it valuable in developing new food products with improved taste profiles.
  • Cosmetic Formulations: The compound is incorporated into cosmetic products for its potential skin benefits, such as improving hydration and skin elasticity, appealing to the growing demand for functional beauty products.

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