(3-(Neopentyloxy)phenyl)boronic acid

96%

Reagent Code: #220220
fingerprint
CAS Number 1236191-14-2

science Other reagents with same CAS 1236191-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.06 g/mol
Formula C₁₁H₁₇BO₃
badge Registry Numbers
MDL Number MFCD18087686
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals due to its stability and reactivity. The neopentyloxy group enhances steric and electronic properties, improving selectivity in coupling processes. Also applied in materials science for designing functional organic molecules and sensors. Its boronic acid functionality allows for reversible interactions with diols, useful in biochemical and sensing applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,700.00
inventory 1g
10-20 days ฿9,890.00
inventory 5g
10-20 days ฿36,810.00
(3-(Neopentyloxy)phenyl)boronic acid
No image available

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals due to its stability and reactivity. The neopentyloxy group enhances steric and electronic properties, improving selectivity in coupling processes. Also applied in materials science for designing functional organic molecules and sensors. Its boronic acid functionality allows for reversible interactions wit

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals due to its stability and reactivity. The neopentyloxy group enhances steric and electronic properties, improving selectivity in coupling processes. Also applied in materials science for designing functional organic molecules and sensors. Its boronic acid functionality allows for reversible interactions with diols, useful in biochemical and sensing applications.

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...