101349-12-6 | 2-(5-Fluoro-1h-indol-3-yl)ethanol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$12.00
5g	98%	in stock	$44.00	$31.00
10g	98%	in stock	$79.00	$56.00

Description

• Catalog Number: AA05343
• Chemical Name: 2-(5-Fluoro-1h-indol-3-yl)ethanol
• CAS Number: 101349-12-6
• Molecular Formula: C10H10FNO
• Molecular Weight: 179.1909
• MDL Number: MFCD09752697
• SMILES: OCCc1c[nH]c2c1cc(F)cc2

Upstream Synthesis Route

2-(5-Fluoro-1H-indol-3-yl)ethanol is a valuable compound widely utilized in chemical synthesis due to its versatile reactivity and unique properties. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. It is particularly valued for its ability to undergo efficient and selective transformations, enabling the rapid synthesis of complex molecular structures.In organic synthesis, 2-(5-Fluoro-1H-indol-3-yl)ethanol can function as a starting material for the synthesis of indole derivatives, which are prevalent motifs in bioactive compounds. By incorporating this compound as a precursor, chemists can introduce specific functional groups at the indole nitrogen or the ethyl side chain, allowing for the generation of diverse analogs with potentially enhanced biological activities.Moreover, the hydroxyl group present in the structure of 2-(5-Fluoro-1H-indol-3-yl)ethanol offers additional synthetic opportunities. This alcohol functionality enables the facile derivatization of the molecule through various chemical reactions, such as esterification, etherification, and oxidation. By strategically modifying this hydroxyl group, researchers can fine-tune the physicochemical properties of the resulting compounds, thus expanding the scope of potential applications in drug discovery and material science.Overall, the strategic incorporation of 2-(5-Fluoro-1H-indol-3-yl)ethanol in chemical synthesis processes opens up a wide range of possibilities for the efficient construction of diverse molecular architectures with tailored functionalities and properties. Its versatile nature and synthetic utility position it as a valuable tool for the design and development of novel compounds with therapeutic, agricultural, and technological applications.