(R)-5-Allyl-2-oxabicyclo[3.3.0]oct-8-ene

≥95%

  • Product Code: 71370
  CAS:    911200-98-1
Molecular Weight: 150.22 g./mol Molecular Formula: C₁₀H₁₄O
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of complex molecules. Its unique bicyclic structure and chiral center make it valuable in the synthesis of pharmaceuticals, where stereochemistry plays a critical role in drug efficacy. It is often employed in the preparation of intermediates for bioactive compounds, including those with potential therapeutic applications in neurological and cardiovascular diseases. Additionally, its allyl group provides a versatile handle for further functionalization, enabling chemists to tailor the molecule for specific synthetic pathways. This compound is also explored in asymmetric catalysis, where it can act as a ligand or precursor to chiral catalysts, enhancing the enantioselectivity of chemical reactions.
Product Specification:
Test Specification
APPEARANCE Colorless to Almost colorless clear liquid
PURITY 95-100
SPECIFIC GRAVITY 2020 0.9810-0.9870
Refractive index n20D 1.4950-1.4990
Specific rotation 20Dc1 MeOH -112--100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days Ft27,581.72
+
-
1.000 10-20 days Ft67,014.95
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-
(R)-5-Allyl-2-oxabicyclo[3.3.0]oct-8-ene
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of complex molecules. Its unique bicyclic structure and chiral center make it valuable in the synthesis of pharmaceuticals, where stereochemistry plays a critical role in drug efficacy. It is often employed in the preparation of intermediates for bioactive compounds, including those with potential therapeutic applications in neurological and cardiovascular diseases. Additionally, its allyl group provides a versatile handle for further functionalization, enabling chemists to tailor the molecule for specific synthetic pathways. This compound is also explored in asymmetric catalysis, where it can act as a ligand or precursor to chiral catalysts, enhancing the enantioselectivity of chemical reactions.
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