(3-Cyclopropylphenyl)boronic acid

95%

Reagent Code: #113217
fingerprint
CAS Number 1049730-10-0

science Other reagents with same CAS 1049730-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.99 g/mol
Formula C₉H₁₁BO₂
badge Registry Numbers
MDL Number MFCD11110340
thermostat Physical Properties
Boiling Point 333.0±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

(3-Cyclopropylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of biologically active compounds. Additionally, it is utilized in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates. Its stability and reactivity make it a versatile tool in research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,435.00
inventory 100mg
10-20 days ฿3,789.00
inventory 1g
10-20 days ฿17,352.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3-Cyclopropylphenyl)boronic acid
No image available

(3-Cyclopropylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of biologically active compounds. Additionally, it is utilized in the development of sensors and catalysts due to

(3-Cyclopropylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of biologically active compounds. Additionally, it is utilized in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates. Its stability and reactivity make it a versatile tool in research and industrial 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...