tert-Butyl 4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamoyl)piperazine-1-carboxylate

98%

Reagent Code: #91116
fingerprint
CAS Number 1704068-57-4

science Other reagents with same CAS 1704068-57-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.34 g/mol
Formula C₂₂H₃₄BN₃O₅
badge Registry Numbers
MDL Number MFCD28805781
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the development of biologically active compounds, aiding in the creation of potential drug candidates. Its piperazine moiety further enhances its utility in medicinal chemistry, as it is often incorporated into molecules to improve pharmacokinetic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿35,870.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamoyl)piperazine-1-carboxylate
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the development of biologically active compounds, aiding in the creation of potential drug candidates. Its piperazine moiety further enhances its

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the development of biologically active compounds, aiding in the creation of potential drug candidates. Its piperazine moiety further enhances its utility in medicinal chemistry, as it is often incorporated into molecules to improve pharmacokinetic properties.

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...