3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethoxy)benzaldehyde

95%

Reagent Code: #117431
fingerprint
CAS Number 1112209-48-9

science Other reagents with same CAS 1112209-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.08 g/mol
Formula C₁₄H₁₆BF₃O₄
badge Registry Numbers
MDL Number MFCD13181638
inventory_2 Storage & Handling
Density 1.23 g/cm3
Storage 2-8°C, inert gas

description Product Description

This chemical, bearing an aldehyde group along with a boronate ester and trifluoromethoxy substituent, is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable building block for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The aldehyde allows for additional transformations like condensations or reductions, while the trifluoromethoxy group enhances its utility in creating compounds with improved metabolic stability and bioavailability. It is often employed in the development of active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its unique structure allows for the introduction of trifluoromethoxy-substituted aromatic rings into target molecules, which is beneficial in drug discovery and material science applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,548.00
inventory 1g
10-20 days ฿7,083.00
inventory 250mg
10-20 days ฿2,628.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethoxy)benzaldehyde
No image available

This chemical, bearing an aldehyde group along with a boronate ester and trifluoromethoxy substituent, is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable building block for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The aldehyde allows for additional transformations like condensations or reductions, while the trifluoromethoxy gro

This chemical, bearing an aldehyde group along with a boronate ester and trifluoromethoxy substituent, is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable building block for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The aldehyde allows for additional transformations like condensations or reductions, while the trifluoromethoxy group enhances its utility in creating compounds with improved metabolic stability and bioavailability. It is often employed in the development of active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its unique structure allows for the introduction of trifluoromethoxy-substituted aromatic rings into target molecules, which is beneficial in drug discovery and material science applications.

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...