5-Methyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

98%

Reagent Code: #203010
fingerprint
CAS Number 1072709-32-0

science Other reagents with same CAS 1072709-32-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.18 g/mol
Formula C₁₅H₂₅BN₂O₃
badge Registry Numbers
MDL Number MFCD22572261
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. The presence of the boronate ester group allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules. Its protected pyrazole ring offers stability during reaction sequences and can be deprotected to reveal active nitrogen functionalities later in the synthesis. This compound is particularly useful in medicinal chemistry for constructing substituted pyrazole derivatives, which are common motifs in bioactive compounds and drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,220.00
inventory 1g
10-20 days ฿27,500.00
5-Methyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
No image available

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. The presence of the boronate ester group allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules. Its protected pyrazole ring offers stability during reaction sequences and can be deprotected to reveal active nitrogen funct

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. The presence of the boronate ester group allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules. Its protected pyrazole ring offers stability during reaction sequences and can be deprotected to reveal active nitrogen functionalities later in the synthesis. This compound is particularly useful in medicinal chemistry for constructing substituted pyrazole derivatives, which are common motifs in bioactive compounds and drug candidates.

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...