(S)-6,6'-Dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diol
≥95%,99%e.e.
- Product Code: 65658
CAS:
1621066-74-7
| Molecular Weight: | 410.1 g./mol | Molecular Formula: | C₁₇H₁₄Br₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 449.2±45.0 °C | |
| Density: | 1.91±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the construction of complex molecules. Its unique spirocyclic structure and bromine substituents make it valuable for creating stereochemically defined intermediates, particularly in the development of pharmaceuticals and agrochemicals. The presence of hydroxyl groups further enhances its reactivity, enabling its use in coupling reactions and as a precursor for further functionalization. Additionally, its chiral nature allows it to play a role in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿45,190.00 |
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(S)-6,6'-Dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diol
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the construction of complex molecules. Its unique spirocyclic structure and bromine substituents make it valuable for creating stereochemically defined intermediates, particularly in the development of pharmaceuticals and agrochemicals. The presence of hydroxyl groups further enhances its reactivity, enabling its use in coupling reactions and as a precursor for further functionalization. Additionally, its chiral nature allows it to play a role in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
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