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

98%

Reagent Code: #117002
fingerprint
CAS Number 848357-46-0

science Other reagents with same CAS 848357-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.12 g/mol
Formula C₁₅H₁₈BNO₆
badge Registry Numbers
MDL Number MFCD11616319
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds. The boronic acid moiety enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the production of biologically active molecules, including potential drug candidates. Additionally, its tert-butoxycarbonyl (Boc) and methoxycarbonyl protecting groups enhance its stability and reactivity during multi-step synthetic processes, allowing for precise modifications in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,767.00

Cart

No products

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

This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds. The boronic acid moiety enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the production of biologically active molecules, including potential drug candidates. Additionally, it

This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds. The boronic acid moiety enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the production of biologically active molecules, including potential drug candidates. Additionally, its tert-butoxycarbonyl (Boc) and methoxycarbonyl protecting groups enhance its stability and reactivity during multi-step synthetic processes, allowing for precise modifications in medicinal chemistry research.

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...