5-(iso-Propyl)furan-2-boronic acid

95%

Reagent Code: #92253
fingerprint
CAS Number 1694670-71-7

science Other reagents with same CAS 1694670-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.97144 g/mol
Formula C₇H₁₁BO₃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the creation of complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Its boronic acid group allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of furan derivatives, which are valuable in material science for creating polymers and organic electronic materials. Its stability and reactivity make it a preferred choice for researchers working on fine chemicals and bioactive 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
5-(iso-Propyl)furan-2-boronic acid
No image available

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the creation of complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Its boronic acid group allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of furan derivatives, which are

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the creation of complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Its boronic acid group allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of furan derivatives, which are valuable in material science for creating polymers and organic electronic materials. Its stability and reactivity make it a preferred choice for researchers working on fine chemicals and bioactive 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...