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1189042-70-3

2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Catalog#: AR0075UU  |   CAS#: 1189042-70-3  |   MDL#: MFCD15143593  |   MF: C12H15BFNO4  |   MW: 267.0612

Packsize Purity Price Availability Quantity
100mg 95% $5.00 Global Stock Buy Now Add To Cart
250mg 95% $8.00 Global Stock Buy Now Add To Cart
1g 95% $20.00 Global Stock Buy Now Add To Cart
5g 95% $82.00 Global Stock Buy Now Add To Cart
10g 95% $156.00 Global Stock Buy Now Add To Cart
25g 95% $298.00 Global Stock Buy Now Add To Cart
50g 95% $554.00 Global Stock Buy Now Add To Cart
100g 95% $1,039.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0075UU
Chemical Name 2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number 1189042-70-3
Molecular Formula C12H15BFNO4
Molecular Weight 267.0612
MDL Number MFCD15143593
SMILES CC1(C)OB(OC1(C)C)c1cccc(c1F)[N+](=O)[O-]

2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a valuable reagent in chemical synthesis due to its unique chemical properties. This compound is commonly used as a boronic acid derivative, making it highly versatile in various synthetic transformations. In organic synthesis, 2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a key building block for the introduction of the fluoro-nitrophenyl group into target molecules. The boronic acid functionality allows for efficient cross-coupling reactions with various electrophiles, such as halides or triflates, enabling the rapid construction of complex organic compounds. Furthermore, the tetramethyl substitution pattern on the boron atom imparts sterically hindered properties to the molecule, enhancing its stability and reactivity in various reaction conditions. This feature makes 2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane particularly useful in challenging synthetic transformations where steric effects play a crucial role in controlling regioselectivity and yield.Overall, the application of 2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis offers chemists a powerful tool for the strategic introduction of functional groups and the efficient construction of diverse molecular scaffolds.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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