8-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline

98%

Reagent Code: #131700
fingerprint
CAS Number 1366740-47-7

science Other reagents with same CAS 1366740-47-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.15 g/mol
Formula C₁₆H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD31630334
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions to construct biaryl and heteroaryl frameworks. Its quinoline core with a methyl substituent enhances electronic and steric properties, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials such as organic light-emitting diodes (OLEDs). The pinacol boronate group offers stability and ease of handling, facilitating its use in iterative synthesis and library generation for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,910.00
inventory 250mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿13,300.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
8-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
No image available

Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions to construct biaryl and heteroaryl frameworks. Its quinoline core with a methyl substituent enhances electronic and steric properties, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials such as organic light-emitting diodes (OLEDs). The pinacol boronate group offers stability and ease of handling, facilitating its use in iterative synthesis and library ge

Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions to construct biaryl and heteroaryl frameworks. Its quinoline core with a methyl substituent enhances electronic and steric properties, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials such as organic light-emitting diodes (OLEDs). The pinacol boronate group offers stability and ease of handling, facilitating its use in iterative synthesis and library generation for drug discovery.

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...