N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide

98%

Reagent Code: #218565
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CAS Number 305448-92-4

science Other reagents with same CAS 305448-92-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.1782 g/mol
Formula C₁₃H₂₀BNO₄S
badge Registry Numbers
MDL Number MFCD05663881
thermostat Physical Properties
Melting Point 153 - 157 ℃ - lit.
Boiling Point 421.7 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.19 g/cm3
Storage Room temperature

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, while the sulfonamide moiety enhances solubility and stability during reaction processes. It is especially valuable in the preparation of biaryl derivatives and functionalized anilines, which are common structural motifs in drug discovery. Its compatibility with various functional groups makes it a versatile building block in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,700.00
inventory 5g
10-20 days ฿7,940.00
N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, while the sulfonamide moiety enhances solubility and stability during reaction processes. It is especially valuable in the preparation of biaryl derivatives and functionalized anilines, which

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, while the sulfonamide moiety enhances solubility and stability during reaction processes. It is especially valuable in the preparation of biaryl derivatives and functionalized anilines, which are common structural motifs in drug discovery. Its compatibility with various functional groups makes it a versatile building block in modern synthetic chemistry.

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