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Catalog Number:
05888
CAS Number:
218938-66-0
L-Aspartic acid β-tert-butyl ester α-allyl ester hydrochloride
Purity:
≥ 98% (NMR)
Synonym(s):
L-Asp(OtBu)-OAll·HCl
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Product Information

L-Aspartic acid b-tert-butyl ester a-allyl ester hydrochloride is a versatile compound widely utilized in the fields of organic synthesis and pharmaceutical development. This compound serves as an important building block for the synthesis of various bioactive molecules, particularly in the design of peptide-based drugs. Its unique structure, featuring both tert-butyl and allyl groups, enhances its reactivity and stability, making it an ideal candidate for applications in medicinal chemistry and agrochemical formulations. Researchers appreciate its ability to facilitate the formation of complex molecular architectures, which can lead to the discovery of novel therapeutic agents.

In addition to its synthetic utility, L-Aspartic acid b-tert-butyl ester a-allyl ester hydrochloride is also recognized for its potential in the development of advanced materials. Its properties allow for the modification of polymeric systems, thereby improving their performance in various applications, including drug delivery and tissue engineering. The compound's favorable characteristics, such as solubility and compatibility with other reagents, position it as a valuable resource for both academic and industrial researchers seeking innovative solutions in chemical synthesis and material science.

Synonyms
L-Asp(OtBu)-OAll·HCl
CAS Number
218938-66-0
Purity
≥ 98% (NMR)
Molecular Formula
C11H19NO4·HCl
Molecular Weight
265.76
MDL Number
MFCD00798679
PubChem ID
129900000
Appearance
Yellow solid
Optical Rotation
[a]D20 = +4.7 to +6.75º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
L-Asp(OtBu)-OAll·HCl
CAS Number
218938-66-0
Purity
≥ 98% (NMR)
Molecular Formula
C11H19NO4·HCl
Molecular Weight
265.76
MDL Number
MFCD00798679
PubChem ID
129900000
Appearance
Yellow solid
Optical Rotation
[a]D20 = +4.7 to +6.75º (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

L-Aspartic acid b-tert-butyl ester a-allyl ester hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Amino Acid Derivatives: It is used to create amino acid derivatives that are essential in peptide synthesis, which is crucial for developing new therapeutic agents.
  • Biotechnology: The compound plays a role in biotechnological applications, including the production of bioactive peptides that can enhance health and nutrition.
  • Cosmetic Formulations: It is incorporated into cosmetic products for its moisturizing properties, improving skin hydration and texture.
  • Research Applications: In academic and industrial research, it is used as a building block for studying metabolic pathways and enzyme functions related to amino acids.

Citations