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Catalog Number:
14469
CAS Number:
143679-80-5
(1S,2S)-Boc-aminocyclopentane carboxylic acid
Purity:
≥ 96% (HPLC)
Synonym(s):
(1S,2S)-Boc-Acpc, (1S,2S)-Boc-2-aminocyclopentane carboxylic acid
Documents
$79.22 /100MG
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Product Information

(1S,2S)-Boc-aminocyclopentane carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound features a unique bicyclic structure that enhances its reactivity and selectivity in various chemical reactions, making it an excellent building block for the synthesis of complex molecules. Its Boc (tert-butyloxycarbonyl) protecting group is particularly advantageous for researchers looking to protect amine functionalities during multi-step synthesis processes.

In practical applications, (1S,2S)-Boc-aminocyclopentane carboxylic acid is often employed in the development of bioactive compounds and pharmaceuticals, especially in the synthesis of peptide analogs and other nitrogen-containing heterocycles. Its ability to facilitate the introduction of amine groups into target molecules allows for the creation of compounds with enhanced biological activity. Researchers appreciate its stability and ease of handling, which contribute to efficient laboratory workflows. With its promising applications in medicinal chemistry and materials science, this compound stands out as a valuable asset for professionals seeking innovative solutions in their projects.

Synonyms
(1S,2S)-Boc-Acpc, (1S,2S)-Boc-2-aminocyclopentane carboxylic acid
CAS Number
143679-80-5
Purity
≥ 96% (HPLC)
Molecular Formula
C11H19NO4
Molecular Weight
229.28
MDL Number
MFCD04974224
PubChem ID
3564732
Appearance
White solid
Optical Rotation
[a]D25 = +38 to +48º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
(1S,2S)-Boc-Acpc, (1S,2S)-Boc-2-aminocyclopentane carboxylic acid
CAS Number
143679-80-5
Purity
≥ 96% (HPLC)
Molecular Formula
C11H19NO4
Molecular Weight
229.28
MDL Number
MFCD04974224
PubChem ID
3564732
Appearance
White solid
Optical Rotation
[a]D25 = +38 to +48º (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

(1S,2S)-Boc-aminocyclopentane carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of peptide-based drugs, enhancing their efficacy and stability.
  • Organic Synthesis: It is employed in organic synthesis as a chiral building block, allowing researchers to create complex molecules with specific stereochemistry, which is crucial in drug design.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and targeting of therapeutic agents.
  • Research in Material Science: It finds applications in the development of new materials, particularly in creating polymers with specific properties, which can be tailored for various industrial applications.
  • Analytical Chemistry: The compound is utilized as a standard in analytical methods, aiding in the quantification and analysis of similar compounds in various samples, ensuring accuracy in research findings.

Citations