2-(4-(Chloromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #83940
fingerprint
CAS Number 1072945-04-0

science Other reagents with same CAS 1072945-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.54 g/mol
Formula C₁₃H₁₈BClO₂
badge Registry Numbers
MDL Number MFCD11053893
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The chloromethyl group further enhances its reactivity, allowing for additional functionalization or modification in complex molecular structures. It is also employed in the development of polymers and organic electronics, where precise molecular design is critical. Its stability and reactivity make it a preferred choice for researchers and industrial chemists working on innovative chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,024.00
inventory 250mg
10-20 days ฿4,536.00
inventory 1g
10-20 days ฿11,322.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(4-(Chloromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
No image available

This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The chloromethyl group further enhances its reactivity, allowing for additional functionalization or modification in complex molecular structures. It is also employed in the development of polymers

This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The chloromethyl group further enhances its reactivity, allowing for additional functionalization or modification in complex molecular structures. It is also employed in the development of polymers and organic electronics, where precise molecular design is critical. Its stability and reactivity make it a preferred choice for researchers and industrial chemists working on innovative chemical 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...