1008105-70-1

Basic information

• Product Name: 2-(1-hydroxy-3-phenylprop-2-yn-1-yl)-4-nitrophenol
• Synonyms: 2-(1-hydroxy-3-phenylprop-2-yn-1-yl)-4-nitrophenol
• CAS NO: 1008105-70-1
• Molecular Weight: 269.257
• Mol File: 1008105-70-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(1-hydroxy-3-phenylprop-2-yn-1-yl)-4-nitrophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-hydroxy-3-phenylprop-2-yn-1-yl)-4-nitrophenol(1008105-70-1)
• EPA Substance Registry System: 2-(1-hydroxy-3-phenylprop-2-yn-1-yl)-4-nitrophenol(1008105-70-1)

Safety Data

• Hazardous Substances Data: 1008105-70-1(Hazardous Substances Data)

Upstream product

• 100-02-7 4-nitro-phenol 
• 97-51-8 5-Nitrosalicylaldehyde 
• 536-74-3 phenylacetylene 

Downstream Products

• 1008105-80-3 (Z)-2-benzylidene-5-nitro-2,3-dihydrobenzofuran-3-ol 
• 131948-12-4 6-Nitroflavone 
• 886-66-8 1,4-diphenyl-1,3-butadiyne 
• 97-51-8 5-Nitrosalicylaldehyde 
• 1384475-78-8 C₁₅H₁₁NO₄ 
• 131948-11-3 (Z)-5-nitroaurone 

Relevant articles and documents

Metal-Free One-Pot Synthesis of 3-Phosphinoylbenzofurans via Phospha-Michael Addition/Cyclization of H-Phosphine Oxides and in Situ Generated ortho-Quinone Methides

A novel metal-free one-pot protocol for the effective and efficient synthesis of 3-phosphinoylbenzofurans via a phospha-Michael addition/cyclization of H-phosphine oxides and in situ generated ortho-quinone methides is described. Based on the expeditious

Synthesis of chromones through LiOtBu/air-mediated oxidation and regioselective cyclization of o-hydroxyphenyl propargyl carbinols

A cascade oxidative cyclization reaction for the synthesis of chromone derivatives was developed by using LiOtBu as a mediator and air as an oxidant. The reaction was carried out without the assistance of a transition metal under mild conditions to afford the chromones in good yields with high regioselectivities. A tandem reaction for the synthesis of various chromones was developed. LiOtBu was used as a mediator and air was used as a clean oxidant. The reaction generally showed high regioselectivity under mild conditions. Extensive research showed that dehydrogenative oxidation of the alcohols under strongly basic conditions was the crucial step, and Li+ was also found to play an important role in this process. Copyright

Versatile and expeditious synthesis of aurones via AuI-catalyzed cyclization

(Chemical Equation Presented) Aurones are conveniently formed in a three-step procedure including a goldI-catalyzed cyclization of 2-(1-hydroxyprop-2-ynyl)phenols as a highly regio- and stereoselective key step. A wide diversity of derivatives can be obtained starting from substituted salicylaldehydes. Synthesis of natural 4,6,3′,4′-tetramethoxyaurone and structure revision of two natural products (dalmaisione D and 4′-chloroaurone) were achieved.