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Catalog Number:
29624
CAS Number:
676629-90-6
(S)-Boc-2-amino-3,3-dimethyl-pent-4-enoic acid
Purity:
≥ 99.5% (Chiral HPLC)
Documents
$106.96 /25MG
Pack Size Availability Price
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Product Information

(S)-Boc-2-amino-3,3-dimethyl-pent-4-enoic acid is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical development. This amino acid derivative, characterized by its Boc (tert-butyloxycarbonyl) protecting group, offers enhanced stability and ease of handling, making it an ideal choice for researchers engaged in peptide synthesis and drug formulation. Its unique structure allows for selective reactions, facilitating the creation of complex molecules with high specificity.

In addition to its applications in peptide chemistry, (S)-Boc-2-amino-3,3-dimethyl-pent-4-enoic acid serves as a valuable building block in the synthesis of biologically active compounds, including potential pharmaceuticals and agrochemicals. Its ability to participate in various coupling reactions expands its utility in medicinal chemistry, where it can be employed to develop novel therapeutic agents. Researchers appreciate its favorable properties, such as solubility and reactivity, which contribute to efficient synthesis processes and improved yields in laboratory settings.

CAS Number
676629-90-6
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C12H21NO4
Molecular Weight
243.3
MDL Number
MFCD18762151
PubChem ID
11368519
Appearance
White solid
Optical Rotation
[a]D20 = 10 ± 2 º (C=1 in MeOH)
Conditions
Store at ≤ - 4 °C
General Information
CAS Number
676629-90-6
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C12H21NO4
Molecular Weight
243.3
MDL Number
MFCD18762151
PubChem ID
11368519
Appearance
White solid
Optical Rotation
[a]D20 = 10 ± 2 º (C=1 in MeOH)
Conditions
Store at ≤ - 4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Boc-2-amino-3,3-dimethyl-pent-4-enoic acid 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 pharmaceutical industry where custom peptides are developed for therapeutic applications.
  • Drug Development: It is instrumental in the design of new drugs, especially those targeting specific biological pathways, due to its unique structural properties that enhance binding affinity.
  • Biotechnology: In biotechnological applications, it is used to create modified amino acids that can improve the stability and efficacy of biologics, making treatments more effective.
  • Research in Molecular Biology: Researchers utilize this compound to study protein interactions and functions, providing insights that can lead to breakthroughs in understanding diseases.
  • Cosmetic Formulations: Its properties also find applications in the cosmetic industry, where it can be used in formulations aimed at improving skin health and appearance.

Citations