6-Methyl-2-(naphthalen-2-yl)-1,3,6,2-dioxazaborocane-4,8-dione

98%

Reagent Code: #208532
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CAS Number 1257648-36-4

science Other reagents with same CAS 1257648-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.09 g/mol
Formula C₁₅H₁₄BNO₄
badge Registry Numbers
MDL Number MFCD11215218
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the resolution and analysis of enantiomeric mixtures. Its boron-containing heterocyclic structure enables coordination with nucleophiles, making it valuable in catalytic cycles for stereoselective transformations. Commonly applied in the pharmaceutical industry to control stereochemistry during the synthesis of bioactive molecules. Also serves as a building block in the development of boron-based sensors and functional materials due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,120.00
inventory 5g
10-20 days ฿12,100.00
inventory 25g
10-20 days ฿42,340.00

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6-Methyl-2-(naphthalen-2-yl)-1,3,6,2-dioxazaborocane-4,8-dione
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Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the resolution and analysis of enantiomeric mixtures. Its boron-containing heterocyclic structure enables coordination with nucleophiles, making it valuable in catalytic cycles for stereoselective transformations. Commonly applied in the pharmaceutical industry to control stereochemistry during the synthesis of bioactive molecules. Also serves as a building block in the development of boron-based sensors and functional materials

Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the resolution and analysis of enantiomeric mixtures. Its boron-containing heterocyclic structure enables coordination with nucleophiles, making it valuable in catalytic cycles for stereoselective transformations. Commonly applied in the pharmaceutical industry to control stereochemistry during the synthesis of bioactive molecules. Also serves as a building block in the development of boron-based sensors and functional materials due to its stability and reactivity profile.

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