(1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one

95%

  • Product Code: 36104
  Alias:    (1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one
  CAS:    79200-56-9
Molecular Weight: 109.13 g./mol Molecular Formula: C₆H₇NO
EC Number: 418-530-1 MDL Number:
Melting Point: 94-97 °C(lit.) Boiling Point: 319.3ºC at 760 mmHg
Density: 1.198 g/cm3 Storage Condition: 2~8°C
Product Description: (1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one is a versatile chemical compound with significant applications in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active molecules, particularly in the development of chiral compounds. Its bicyclic structure and functional groups make it a valuable building block for synthesizing complex molecules, including those used in medicinal chemistry for drug discovery. The compound is often employed in asymmetric synthesis, where its rigid framework helps control stereochemistry, leading to the creation of enantiomerically pure substances. Additionally, it is utilized in the preparation of ligands for catalysis and in the study of enzyme inhibitors, contributing to advancements in therapeutic agents and chemical processes.
Product Specification:
Test Specification
PURITY GC 94.5 100%
Appearance White to Tan Powder or Crystal or Chunk(s)
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿350.00
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5.000 10-20 days ฿840.00
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25.000 10-20 days ฿3,150.00
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(1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one
(1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one is a versatile chemical compound with significant applications in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active molecules, particularly in the development of chiral compounds. Its bicyclic structure and functional groups make it a valuable building block for synthesizing complex molecules, including those used in medicinal chemistry for drug discovery. The compound is often employed in asymmetric synthesis, where its rigid framework helps control stereochemistry, leading to the creation of enantiomerically pure substances. Additionally, it is utilized in the preparation of ligands for catalysis and in the study of enzyme inhibitors, contributing to advancements in therapeutic agents and chemical processes.
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