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Catalog Number:
15399
CAS Number:
270263-02-0
L-β-Homoallylglycine hydrochloride
Purity:
≥ 98% (NMR)
Synonym(s):
L-β-HomoGly(allyl)-OH·HCl, (S-3-Amino-5-hexenoic acid hydrochloride
Documents
$120.88 /100MG
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Product Information

L-b-Homoallylglycine hydrochloride is a versatile amino acid derivative that has garnered attention in various fields of research and industry. This compound is recognized for its unique structural properties, which make it an excellent candidate for applications in peptide synthesis and as a building block in medicinal chemistry. Its ability to serve as a chiral auxiliary enhances its utility in asymmetric synthesis, allowing researchers to create compounds with specific stereochemistry. Additionally, L-b-Homoallylglycine hydrochloride has shown potential in neurochemical studies, particularly in the modulation of neurotransmitter systems, which can lead to advancements in drug development for neurological disorders.

Researchers and industry professionals can leverage L-b-Homoallylglycine hydrochloride in the development of novel therapeutic agents, especially in the fields of neuropharmacology and organic synthesis. Its stability and reactivity make it a valuable tool for creating complex molecules with desired biological activities. With its growing relevance in scientific research, L-b-Homoallylglycine hydrochloride stands out as a promising compound for those looking to innovate in drug discovery and development.

Synonyms
L-β-HomoGly(allyl)-OH·HCl, (S-3-Amino-5-hexenoic acid hydrochloride
CAS Number
270263-02-0
Purity
≥ 98% (NMR)
Molecular Formula
C6H11NO2·HCl
Molecular Weight
165.62
MDL Number
MFCD01861086
PubChem ID
53397996
Appearance
White to off-white powder
Optical Rotation
[α]D25 = +18.0 ± 2º (C=1 in H2O)
Conditions
Store at 0-8°C
General Information
Synonyms
L-β-HomoGly(allyl)-OH·HCl, (S-3-Amino-5-hexenoic acid hydrochloride
CAS Number
270263-02-0
Purity
≥ 98% (NMR)
Molecular Formula
C6H11NO2·HCl
Molecular Weight
165.62
MDL Number
MFCD01861086
PubChem ID
53397996
Appearance
White to off-white powder
Optical Rotation
[α]D25 = +18.0 ± 2º (C=1 in H2O)
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

L-b-Homoallylglycine hydrochloride is widely utilized in research focused on:

  • Neuroscience Research: This compound serves as a valuable tool in studying neurotransmitter systems, particularly in the modulation of glutamate receptors, which are crucial for understanding various neurological disorders.
  • Drug Development: It plays a significant role in the synthesis of novel pharmaceutical compounds, aiding researchers in developing new medications that target specific biological pathways.
  • Peptide Synthesis: This chemical is used in the synthesis of peptides, enhancing the stability and bioactivity of peptide-based drugs, which is particularly beneficial in therapeutic applications.
  • Biochemical Assays: L-b-Homoallylglycine hydrochloride is employed in various biochemical assays to investigate enzyme activity and protein interactions, providing insights into metabolic pathways.
  • Academic Research: It is commonly used in academic settings for teaching and research purposes, helping students and researchers explore amino acid derivatives and their functionalities in biological systems.

Citations