(E)-2-(2-Methoxystyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #184521
fingerprint
CAS Number 149777-81-1

science Other reagents with same CAS 149777-81-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.1371 g/mol
Formula C₁₅H₂₁BO₃
badge Registry Numbers
MDL Number MFCD19703870
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical, agrochemical, and materials science research. The presence of the methoxystyryl moiety allows for the construction of conjugated systems, often found in optoelectronic materials and bioactive compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,180.00
inventory 250mg
10-20 days ฿25,620.00
inventory 1g
10-20 days ฿51,250.00

Cart

No products

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

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical, agrochemical, and materials science research. The presence of the methoxystyryl moiety allows for the construction of conjugated systems, often found in optoelectronic materi

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical, agrochemical, and materials science research. The presence of the methoxystyryl moiety allows for the construction of conjugated systems, often found in optoelectronic materials and bioactive compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug development.

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...