1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(thiophen-2-ylmethyl)urea

95%

Reagent Code: #89459
fingerprint
CAS Number 874301-80-1

science Other reagents with same CAS 874301-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.26282 g/mol
Formula C₁₈H₂₃BN₂O₃S
badge Registry Numbers
MDL Number MFCD32206522
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronate ester group in its structure makes it valuable for Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds efficiently. Additionally, its urea moiety can contribute to the biological activity of the final compounds, making it useful in drug discovery for targeting specific enzymes or receptors. Its application extends to materials science, where it can be employed in the synthesis of organic electronic materials due to the presence of the thiophene group, which is known for its conductive properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿6,462.00
inventory 250mg
10-20 days ฿25,650.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(thiophen-2-ylmethyl)urea
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronate ester group in its structure makes it valuable for Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds efficiently. Additionally, its urea moiety can contribute to the biological activity of the final compounds, ma

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronate ester group in its structure makes it valuable for Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds efficiently. Additionally, its urea moiety can contribute to the biological activity of the final compounds, making it useful in drug discovery for targeting specific enzymes or receptors. Its application extends to materials science, where it can be employed in the synthesis of organic electronic materials due to the presence of the thiophene group, which is known for its conductive 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...