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

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Reagent Code: #68655
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CAS Number 1456816-37-7

science Other reagents with same CAS 1456816-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 370.42 g/mol
Formula C₂₅H₂₃OP
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MDL Number MFCD31630705
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,437.00
inventory 250mg
10-20 days ฿10,485.00
inventory 1g
10-20 days ฿27,279.00

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

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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