(1-(tert-Butoxycarbonyl)-6-fluoro-1H-indol-2-yl)boronic acid

98%

Reagent Code: #39715
fingerprint
CAS Number 1000068-26-7

science Other reagents with same CAS 1000068-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.0700 g/mol
Formula C₁₃H₁₅BFNO₄
badge Registry Numbers
MDL Number MFCD09953519
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound 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 molecules, especially in pharmaceutical research. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable for constructing indole-based compounds. These compounds are often explored for their potential biological activities, including drug development for treating various diseases. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating controlled synthesis processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,538.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(1-(tert-Butoxycarbonyl)-6-fluoro-1H-indol-2-yl)boronic acid
No image available

This compound 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 molecules, especially in pharmaceutical research. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable for constructing indole-based compounds. These compounds are often explored for their potential biological activities, including drug development for treating various d

This compound 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 molecules, especially in pharmaceutical research. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable for constructing indole-based compounds. These compounds are often explored for their potential biological activities, including drug development for treating various diseases. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating controlled synthesis processes.

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...