(1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroquinolin-7-yl)boronic acid

98%

Reagent Code: #131281
fingerprint
CAS Number 1926137-46-3

science Other reagents with same CAS 1926137-46-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.12 g/mol
Formula C₁₄H₂₀BNO₄
badge Registry Numbers
MDL Number MFCD20441850
thermostat Physical Properties
Boiling Point 443.5±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in complex organic structures. Commonly employed in medicinal chemistry for constructing drug candidates targeting cancer and inflammatory diseases. The tert-butoxycarbonyl (Boc) group provides amine protection during synthesis, enhancing stability and selectivity in multi-step reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,520.00
inventory 100mg
10-20 days ฿12,070.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroquinolin-7-yl)boronic acid
No image available

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in complex organic structures. Commonly employed in medicinal chemistry for constructing drug candidates targeting cancer and inflammatory diseases. The tert-butoxycarbonyl (Boc) group provides amine protection during synthesis, enhancing sta

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in complex organic structures. Commonly employed in medicinal chemistry for constructing drug candidates targeting cancer and inflammatory diseases. The tert-butoxycarbonyl (Boc) group provides amine protection during synthesis, enhancing stability and selectivity in multi-step reactions.

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...