tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

≥97%

Reagent Code: #90934
fingerprint
CAS Number 893566-72-8

science Other reagents with same CAS 893566-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.27 g/mol
Formula C₂₀H₃₀BNO₄
badge Registry Numbers
MDL Number MFCD11044669
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group provides protection for the amine functionality during synthetic processes, ensuring selective reactivity. Its application is significant in medicinal chemistry for the development of drug candidates and bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,040.00
inventory 1g
10-20 days ฿23,220.00
inventory 250mg
10-20 days ฿8,640.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group provides protection for the amine fu

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group provides protection for the amine functionality during synthetic processes, ensuring selective reactivity. Its application is significant in medicinal chemistry for the development of drug candidates and bioactive compounds.

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...