118172-64-8

Basic information

• Product Name: 2-(4-hydroxy-3-nitrophenyl)ethanol
• Synonyms: 2-(4-hydroxy-3-nitrophenyl)ethanol
• CAS NO: 118172-64-8
• Molecular Weight: 183.164
• Mol File: 118172-64-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(4-hydroxy-3-nitrophenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-hydroxy-3-nitrophenyl)ethanol(118172-64-8)
• EPA Substance Registry System: 2-(4-hydroxy-3-nitrophenyl)ethanol(118172-64-8)

Safety Data

• Hazardous Substances Data: 118172-64-8(Hazardous Substances Data)

Upstream product

• 104-10-9 2-(4'-aminophenyl)ethyl alcohol 
• 119-10-8 4-methoxy-3-nitrotoluene 
• 106-44-5 p-cresol 
• 104-93-8 p-methylanizole 
• 168766-14-1 2-(4-methoxy-3-nitrophenyl)ethanol 
• 501-94-0 p-hydroxyphenethyl alcohol 

Downstream Products

• 346730-62-9 C₂₀H₁₅N₃O₁₂S₂ 
• 118172-66-0 2-(3-amino-4-hydroxyphenyl)ethanol 

Relevant articles and documents

Tyrosol-biotin small molecular probe as well as preparation method and application thereof

The invention discloses a tyrosol-biotin small molecular probe as well as a preparation method and application thereof. The structural formula of the tyrosol small molecular probe comprises tyrosol, biotin and a connecting chain. In-vitro activity tests s

Iodine(III)-Catalyzed Electrophilic Nitration of Phenols via Non-Br?nsted Acidic NO2+ Generation

The first catalytic procedure for the electrophilic nitration of phenols was developed using iodosylbenzene as an organocatalyst based on iodine(III) and aluminum nitrate as a nitro group source. This atom-economic protocol occurs under mild, non-Br?nsted acidic and open-flask reaction conditions with a broad functional-group tolerance including several heterocycles. Density functional theory (DFT) calculations at the (SMD:MeCN)Mo8-HX/(LANLo8+f,6-311+G) level indicated that the reaction proceeds through a cationic pathway that efficiently generates the NO2+ ion, which is the nitrating species under neutral conditions.

Steroid and nitro phenol esters from Bignonia unguis-cati roots

Two new esters, β-sitosterol cerotate 1 and 2-(4-hydroxy-3-nitrophenyl)ethyl stearate 2 have been isolated from the roots of Bignonia unguis-cati (Bignoniaceae) and their structures are elucidated by spectroscopic and chemical studies.