(R)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

  • Product Code: 68655
  CAS:    1456816-37-7
Molecular Weight: 370.42 g./mol Molecular Formula: C₂₅H₂₃OP
EC Number: MDL Number: MFCD31630705
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This chemical is primarily utilized in the field of organic synthesis, particularly in the development of chiral catalysts. Its unique structure, featuring an anthracene group and a dihydrobenzooxaphosphole ring, makes it effective in asymmetric synthesis reactions. It is often employed in the production of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for creating drugs with specific biological activities. Additionally, it finds application in material science, where it is used to synthesize advanced organic materials with potential uses in optoelectronics and photovoltaics. Its ability to induce chirality in reactions also makes it valuable in the study of stereochemistry and the development of novel synthetic methodologies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $133.12
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0.250 10-20 days $314.58
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1.000 10-20 days $818.45
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(R)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of chiral catalysts. Its unique structure, featuring an anthracene group and a dihydrobenzooxaphosphole ring, makes it effective in asymmetric synthesis reactions. It is often employed in the production of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for creating drugs with specific biological activities. Additionally, it finds application in material science, where it is used to synthesize advanced organic materials with potential uses in optoelectronics and photovoltaics. Its ability to induce chirality in reactions also makes it valuable in the study of stereochemistry and the development of novel synthetic methodologies.
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