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Catalog Number:
41507
CAS Number:
291775-59-2
Acide (1 R ,3 S ,4 S )- N -Boc-2-azabicyclo[2.2.1]heptane-3-carboxylique
Purity:
≥ 96,5 % (HPLC)
Synonym(s):
Acide (1 R ,3 S ,4 S )-2-(tert-butoxycarbonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylique
Hazmat
Documents
$104.26 /250 mg
Taille
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Product Information

Adapté à la synthèse de peptides

Synonyms
Acide (1 R ,3 S ,4 S )-2-(tert-butoxycarbonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylique
CAS Number
291775-59-2
Purity
≥ 96,5 % (HPLC)
Molecular Formula
C 12 H 19 NON 4
Molecular Weight
0
MDL Number
MFCD11099876
PubChem ID
15056388
Melting Point
147 - 152 °C
Appearance
Solide blanc à beige
Optical Rotation
[ á]22/D = -170 ± 10 ° (C = 1 dans le chloroforme)
Conditions
Magasin chez RT
General Information
Synonyms
Acide (1 R ,3 S ,4 S )-2-(tert-butoxycarbonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylique
CAS Number
291775-59-2
Purity
≥ 96,5 % (HPLC)
Molecular Formula
C 12 H 19 NON 4
Molecular Weight
0
MDL Number
MFCD11099876
PubChem ID
15056388
Melting Point
147 - 152 °C
Appearance
Solide blanc à beige
Optical Rotation
[ á]22/D = -170 ± 10 ° (C = 1 dans le chloroforme)
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(1R,3S,4S)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a versatile building block for synthesizing complex molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique structure allows for the design of novel drug candidates, especially in the field of central nervous system disorders, enhancing the potential for effective treatments.
  • Peptide Synthesis: The compound is used in the preparation of peptide derivatives, which are crucial in creating biologically active compounds for therapeutic applications.
  • Chiral Catalysis: It plays a significant role in asymmetric synthesis, providing chiral centers that are essential for producing enantiomerically pure compounds, which are important in the pharmaceutical industry.
  • Research in Neuroscience: The compound's structural properties make it a candidate for studying receptor interactions, contributing to advancements in understanding neuropharmacology.

Citations