1000068-25-6 | 1-BOC-4-fluoroindole-2-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$29.00	$20.00
250mg	95%	in stock	$60.00	$42.00
500mg	95%	in stock	$107.00	$75.00
1g	95%	in stock	$160.00	$112.00
5g	95%	in stock	$663.00	$464.00
10g	95%	in stock	$1,311.00	$918.00

Description

• Catalog Number: AA00140
• Chemical Name: 1-BOC-4-fluoroindole-2-boronic acid
• CAS Number: 1000068-25-6
• Molecular Formula: C13H15BFNO4
• Molecular Weight: 279.0719
• MDL Number: MFCD11109421
• SMILES: OB(c1cc2c(n1C(=O)OC(C)(C)C)cccc2F)O

Upstream Synthesis Route

(1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid, often referred to as $name$, is a versatile compound widely utilized in organic chemical synthesis. This boronic acid derivative serves as a key building block in the creation of various complex organic molecules due to its unique reactivity and structural characteristics.In chemical synthesis, (1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid is commonly employed as a precursor in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by a palladium catalyst, enables the formation of carbon-carbon bonds between the boronic acid group of $name$ and another organic halide or pseudohalide compound. This versatile coupling reaction allows for the efficient and selective creation of biaryl compounds, which are important structural motifs found in many pharmaceuticals, agrochemicals, and materials.Furthermore, (1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid can also be utilized in the synthesis of indole derivatives, which are prevalent in numerous bioactive compounds and natural products. By incorporating this boronic acid derivative into synthetic pathways, chemists can access a wide range of indole-containing molecules with diverse pharmacological properties and potential therapeutic applications.Overall, the strategic incorporation of (1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid into chemical synthesis processes enables the efficient construction of complex organic structures, making it an invaluable tool for synthetic chemists across various research fields.