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

98%

Reagent Code: #208541
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CAS Number 1311484-45-3

science Other reagents with same CAS 1311484-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.025 g/mol
Formula C₁₁H₁₁BN₂O₆
badge Registry Numbers
MDL Number MFCD11215228
thermostat Physical Properties
Melting Point 211-215℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of boron-containing compounds for pharmaceuticals and agrochemicals. Its structure allows for selective transformations in heterocyclic chemistry, making it valuable in the preparation of bioactive molecules. The presence of both nitro and boron functional groups enables participation in cross-coupling reactions and nitro group reductions, facilitating the construction of complex molecular architectures. Commonly employed in research settings for designing novel therapeutic agents and functional materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,070.00
inventory 5g
10-20 days ฿3,900.00
inventory 25g
10-20 days ฿15,180.00
6-Methyl-2-(3-nitrophenyl)-1,3,6,2-dioxazaborocane-4,8-dione
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Used as an intermediate in organic synthesis, particularly in the development of boron-containing compounds for pharmaceuticals and agrochemicals. Its structure allows for selective transformations in heterocyclic chemistry, making it valuable in the preparation of bioactive molecules. The presence of both nitro and boron functional groups enables participation in cross-coupling reactions and nitro group reductions, facilitating the construction of complex molecular architectures. Commonly employed in re

Used as an intermediate in organic synthesis, particularly in the development of boron-containing compounds for pharmaceuticals and agrochemicals. Its structure allows for selective transformations in heterocyclic chemistry, making it valuable in the preparation of bioactive molecules. The presence of both nitro and boron functional groups enables participation in cross-coupling reactions and nitro group reductions, facilitating the construction of complex molecular architectures. Commonly employed in research settings for designing novel therapeutic agents and functional materials.

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