tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate

98%

Reagent Code: #215143
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CAS Number 1202794-01-1

science Other reagents with same CAS 1202794-01-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.1715 g/mol
Formula C₁₄H₂₆BNO₄
badge Registry Numbers
MDL Number MFCD24466576
inventory_2 Storage & Handling
Density 1.00±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and reactivity profile support its use in multi-step syntheses where selective transformations are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,220.00
inventory 250mg
10-20 days ฿7,480.00
inventory 1g
10-20 days ฿15,700.00
inventory 5g
10-20 days ฿43,300.00

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tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate
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Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and r

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and reactivity profile support its use in multi-step syntheses where selective transformations are required.

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