5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-amine

97%

Reagent Code: #131284
fingerprint
CAS Number 2816090-91-0

science Other reagents with same CAS 2816090-91-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.15 g/mol
Formula C₁₆H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD32644595
thermostat Physical Properties
Boiling Point 433.9±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl and heterobiaryl systems. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of an amine group allows for further functionalization, such as acylation, sulfonylation, or diazotization, enabling diverse molecular derivatization. It is especially useful in the development of conjugated materials for optoelectronics and in the synthesis of complex aromatic amines found in bioactive molecules. Its dual functionality—boronate and amine—supports sequential reaction strategies in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,400.00
inventory 250mg
10-20 days ฿9,940.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-amine
No image available

Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl and heterobiaryl systems. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of an amine group allows for further functionalization, such as acylation, sulfonylation, or diazotization, enabling diverse molecular derivatization.

Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl and heterobiaryl systems. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of an amine group allows for further functionalization, such as acylation, sulfonylation, or diazotization, enabling diverse molecular derivatization. It is especially useful in the development of conjugated materials for optoelectronics and in the synthesis of complex aromatic amines found in bioactive molecules. Its dual functionality—boronate and amine—supports sequential reaction strategies in multi-step syntheses.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...