118573-52-7 | 2-(4-Hydroxy-1H-indol-3-yl)acetonitrile

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	3 weeks	$1,134.00	$794.00
100mg	95%	3 weeks	$1,579.00	$1,105.00
250mg	95%	3 weeks	$2,159.00	$1,511.00
500mg	95%	3 weeks	$3,266.00	$2,287.00

Description

• Catalog Number: AD74420
• Chemical Name: 2-(4-Hydroxy-1H-indol-3-yl)acetonitrile
• CAS Number: 118573-52-7
• Molecular Formula: C10H8N2O
• Molecular Weight: 172.1833
• MDL Number: MFCD12964925
• SMILES: N#CCc1c[nH]c2c1c(O)ccc2

Upstream Synthesis Route

4-Hydroxy-1H-indole-3-acetonitrile, also known as $(name)$, is a key intermediate in chemical synthesis widely utilized in the pharmaceutical and fine chemical industries. This compound serves as a valuable building block in the preparation of various complex organic molecules due to its versatile reactivity and functional group compatibility.One of the prominent applications of $(name)$ in chemical synthesis is its role as a precursor in the synthesis of indole-based pharmaceutical compounds. Indoles are a class of heterocyclic compounds that exhibit diverse biological activities, making them essential components in drug discovery and development. By utilizing $(name)$ as a starting material, chemists can efficiently access structurally diverse indole derivatives through various synthetic transformations.Additionally, $(name)$ can be employed in the synthesis of natural products and bioactive molecules with indole moieties. Its unique chemical structure allows for the introduction of specific functional groups or modifications that are crucial for enhancing the pharmacological properties of the final compound. Through strategic manipulation of the indole ring system, researchers can tailor the properties of the target molecules to achieve desired biological effects.Furthermore, $(name)$ can be utilized in the development of novel materials and organic compounds with potential applications in agrochemicals, dyes, and polymer chemistry. Its versatility as a synthetic intermediate enables chemists to access a diverse array of functionalized indole derivatives, opening up opportunities for the exploration of new chemical entities with tailored properties and applications.In conclusion, 4-Hydroxy-1H-indole-3-acetonitrile plays a pivotal role in chemical synthesis by serving as a key building block for the preparation of indole-based compounds with pharmaceutical, biological, and material science applications. Its reactivity and structural features make it an indispensable tool for organic chemists seeking to create innovative molecules with tailored properties and functions.