1-Dodecylboronic acid pinacol ester

98%

Reagent Code: #175590
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CAS Number 177035-82-4

science Other reagents with same CAS 177035-82-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.3100 g/mol
Formula C₁₈H₃₇BO₂
badge Registry Numbers
MDL Number MFCD12546195
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its lipophilic dodecyl chain enhances solubility in nonpolar solvents, making it valuable in the synthesis of long-chain functionalized compounds. Commonly applied in the development of pharmaceuticals, agrochemicals, and advanced materials where controlled boron-based coupling is required. The pinacol ester group provides stability and ease of handling, allowing for selective transformations under mild conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,090.00
inventory 5g
10-20 days ฿12,350.00

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1-Dodecylboronic acid pinacol ester
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Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its lipophilic dodecyl chain enhances solubility in nonpolar solvents, making it valuable in the synthesis of long-chain functionalized compounds. Commonly applied in the development of pharmaceuticals, agrochemicals, and advanced materials where controlled boron-based coupling is required. The pinacol ester group provides stability and ease of handling, allo

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its lipophilic dodecyl chain enhances solubility in nonpolar solvents, making it valuable in the synthesis of long-chain functionalized compounds. Commonly applied in the development of pharmaceuticals, agrochemicals, and advanced materials where controlled boron-based coupling is required. The pinacol ester group provides stability and ease of handling, allowing for selective transformations under mild conditions.

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