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Catalog Number:
29607
CAS Number:
865689-36-7
Ácido 1S , 2R -Boc-2-aminociclohexanocarboxílico
Purity:
≥ 97% (ensayo)
Synonym(s):
(1 S , 2 R -Boc-Achc
Documents
$93.14 /100 mg
Tamaño
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Product Information

(1S,2R)-Boc-2-aminocyclohexane carboxylic acid is a versatile compound widely utilized in the synthesis of pharmaceuticals and agrochemicals. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is essential for the selective functionalization of amino acids in peptide synthesis. Its unique structure allows for enhanced stability and solubility, making it an excellent choice for researchers focusing on drug development and organic synthesis.

In addition to its application in peptide synthesis, (1S,2R)-Boc-2-aminocyclohexane carboxylic acid is also valuable in the production of chiral intermediates, which are crucial in the formulation of enantiomerically pure drugs. The compound's ability to facilitate the creation of complex molecules with high specificity positions it as a key player in medicinal chemistry and biochemistry. Researchers and industry professionals can leverage its properties to streamline their synthesis processes and improve yields in various applications.

Synonyms
(1 S , 2 R -Boc-Achc
CAS Number
865689-36-7
Purity
≥ 97% (ensayo)
Molecular Formula
C12H21NO4
Molecular Weight
243.3
MDL Number
MFCD06410969
PubChem ID
4405994
Appearance
Polvo blanco
Optical Rotation
[a] D = +20 ± 2º (C=0,5 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(1 S , 2 R -Boc-Achc
CAS Number
865689-36-7
Purity
≥ 97% (ensayo)
Molecular Formula
C12H21NO4
Molecular Weight
243.3
MDL Number
MFCD06410969
PubChem ID
4405994
Appearance
Polvo blanco
Optical Rotation
[a] D = +20 ± 2º (C=0,5 en MeOH)
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

(1S,2R)-Boc-2-aminocyclohexane 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 drugs targeting neurological disorders. Its unique structure allows for the creation of compounds with enhanced bioactivity.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, where its protective Boc group helps in the selective formation of peptide bonds, leading to higher purity and yield of the final product.
  • Chiral Catalysis: The compound's chiral nature makes it valuable in asymmetric synthesis, where it can act as a chiral auxiliary, improving the efficiency and selectivity of reactions in organic chemistry.
  • Material Science: It finds applications in the development of polymers and materials with specific mechanical properties, contributing to advancements in fields like coatings and adhesives.
  • Bioconjugation: This chemical can be used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, which is essential in the development of targeted drug delivery systems and diagnostic tools.

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