Tert-Butyl 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole-1-carboxylate

95%

Reagent Code: #242053
fingerprint
CAS Number 1402174-60-0

science Other reagents with same CAS 1402174-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.18 g/mol
Formula C₁₅H₂₅BN₂O₄
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex imidazole-containing compounds. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) protecting group stabilizes the imidazole nitrogen during reactions and can be easily removed later in the synthesis. This compound is particularly useful in the development of bioactive molecules, including drug candidates targeting enzymes and receptors where imidazole scaffolds are critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿53,110.00
inventory 100mg
10-20 days ฿159,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tert-Butyl 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole-1-carboxylate
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex imidazole-containing compounds. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) protecting group stabilizes the imidazole nitrogen during reactions and can be easily removed later in the synthesis. This compound is particularly useful in the development of bioactive m

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex imidazole-containing compounds. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) protecting group stabilizes the imidazole nitrogen during reactions and can be easily removed later in the synthesis. This compound is particularly useful in the development of bioactive molecules, including drug candidates targeting enzymes and receptors where imidazole scaffolds are critical.

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...