(R)-6,6'-Dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol

≥98%,99%e.e.

  • Product Code: 84849
  CAS:    1286189-15-8
Molecular Weight: 410.10 g./mol Molecular Formula: C₁₇H₁₄Br₂O₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry, sealed
Product Description: This chemical is primarily utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric organic synthesis. Its unique spirobiindene structure and hydroxyl groups make it a valuable building block for creating complex molecules with high enantioselectivity. It is often employed in the development of pharmaceuticals, where precise stereochemistry is crucial for the efficacy and safety of drugs. Additionally, it finds applications in material science, particularly in the design of chiral polymers and advanced materials with specific optical properties. Its role in facilitating stereocontrolled reactions makes it a key component in research and industrial processes aimed at producing enantiomerically pure compounds.
Product Specification:
Test Specification
APPEARANCE White to brown solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days ฿3,600.00
+
-
0.100 10-20 days ฿8,690.00
+
-
0.500 10-20 days ฿28,960.00
+
-
(R)-6,6'-Dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol
This chemical is primarily utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric organic synthesis. Its unique spirobiindene structure and hydroxyl groups make it a valuable building block for creating complex molecules with high enantioselectivity. It is often employed in the development of pharmaceuticals, where precise stereochemistry is crucial for the efficacy and safety of drugs. Additionally, it finds applications in material science, particularly in the design of chiral polymers and advanced materials with specific optical properties. Its role in facilitating stereocontrolled reactions makes it a key component in research and industrial processes aimed at producing enantiomerically pure compounds.
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