3-Cyclopropyl-5-(cyclopentyl)phenylboronic acid

95%

Reagent Code: #91926
fingerprint
CAS Number 2225169-00-4

science Other reagents with same CAS 2225169-00-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.11046 g/mol
Formula C₁₄H₁₉BO₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of materials science, where it contributes to the creation of advanced polymers and functional materials. Its stability and reactivity make it a valuable tool in medicinal chemistry for designing and synthesizing biologically active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿38,322.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Cyclopropyl-5-(cyclopentyl)phenylboronic acid
No image available

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of materials science, where it contributes to the creation of advanced polymers

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of materials science, where it contributes to the creation of advanced polymers and functional materials. Its stability and reactivity make it a valuable tool in medicinal chemistry for designing and synthesizing biologically active 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...