17061-85-7

Basic information

• Product Name: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene
• Synonyms: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene;1-nitro-4-(2-propyn-1-yloxy)Benzene;1-NITRO-4-(2-PROPYNYLOXY)BENZENE
• CAS NO: 17061-85-7
• Molecular Formula: C₉H₇NO₃
• Molecular Weight: 177.15678
• Mol File: 17061-85-7.mol
• Article Data: 78

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene(17061-85-7)
• EPA Substance Registry System: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene(17061-85-7)

Safety Data

• Hazardous Substances Data: 17061-85-7(Hazardous Substances Data)

Usage

Nitroaromatic compound

A type of aromatic compound that contains a nitro group (-NO2) attached to a benzene ring.

Alkyne group

A carbon-carbon triple bond (C≡C) attached to the benzene ring.

Building block for organic synthesis

Used as a starting material in the preparation of various other organic compounds.

Used in pharmaceuticals and agrochemicals

It is used in the production of drugs and chemicals used in agriculture.

Precursor in the synthesis of dyes and pigments

It can be used as a starting material to make dyes and pigments.

Potentially hazardous

It is considered to be potentially dangerous, and proper safety precautions should be taken when handling and using it.

Upstream product

• 100-02-7 4-nitro-phenol 
• 106-96-7 propargyl bromide 
• 1568-66-7 1-allyloxy-4-nitrobenzene 
• 244056-18-6 1-(2-bromoprop-2-en-1-yloxy)-4-nitrobenzene 
• 14670-55-4 1,2-dibromo-3-(4-nitrophenyloxy)propane 
• 1643-19-2 tetrabutylammomium bromide 
• 107-19-7 propargyl alcohol 
• 350-46-9 4-Fluoronitrobenzene 
• 13610-02-1 1-phenoxy-2-propyne 
• 6165-75-9 propargyl benzenesulfonate 

Downstream Products

• 1144040-24-3 1-[2-(2-methyl-5-nitro-imidazol-1-yl)-ethyl]-4-(4-nitro-phenoxymethyl)-1H-[1,2,3]triazole 
• 1391971-20-2 C₁₉H₂₄N₄O₁₄S₂ 
• 1385766-79-9 1-(2-methyl-5-nitrophenyl)-4-((4-nitrophenoxy)methyl)-1H-1,2,3-triazole 
• 1363373-78-7 C₂₁H₂₂N₂O₅ 
• 1363373-77-6 C₁₆H₁₃NO₃ 
• 1363373-76-5 C₁₇H₁₅NO₃ 
• 1363368-20-0 4-(3-(4-aminophenoxy)prop-1-ynyl)-N-((2S,3R)-3-hydroxy-1-(hydroxyamino)-1-oxobutan-2-yI)benzamide 
• 1351982-01-8 5-((4-((4-nitrophenoxy)methyl)-1H-1,2,3-triazol-1-yl)methyl)-2-methylpyrimidin-4-amine 
• 1334667-60-5 1-(4-cyanophenylmethyl)-4-((4-nitrophenoxy)methyl)-1H-1,2,3-triazole 
• 1334667-35-4 1-(4,4'-dicyanodiphenylmethyl)-4-((4-nitrophenoxy)methyl)-1H-1,2,3-triazole 
• 1316708-10-7 N,N-dimethyl-4-(4-nitrophenoxy)but-2-yn-1-amine 
• 66397-25-9 p-Nitrophenyl allenyl ether 
• 1311382-57-6 C₃₅H₃₆N₆O₅S 
• 1311383-39-7 5-(N-(4-((1-benzyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)sulfamoyl)-2-methylbenzoic acid 

Relevant articles and documents

Polymer nanocomposites using click chemistry: Novel materials for hydrogen peroxide vapor sensors

Herein, we report the synthesis of nanocomposites (NCs) prepared by azide-functionalized polystyrene (Az-f-PS) coupled with alkyne-functionalized nanographite platelets (Alk-f-NGPs) by using copper(i) catalyzed azide-alkyne click chemistry. Linear polysty

New phenoxymethyl substituted mesoionic triazolium salts: Synthesis and structural characterisation

A new set of mesoionic 1,2,3-triazolium salts functionalised by para substituted phenoxymethyl side groups were prepared using the ‘click’ Cu catalyzed [3 + 2] cycloaddition of organic azides and terminal alkynes. Four previously unreported neutral triazoles (1–4) were first isolated en route to formation of the salts (5–8). All the compounds were fully characterised (1H, 13C NMR; IR; HR-MS; EA) and representative neutral triazoles and salts were structurally characterised by single crystal X-ray diffraction (SCXRD). Full examination of structural characteristics of the neutral compounds and the salts were presented by detailed analysis of multinuclear NMR data and SCXRD. As metal-free catalysts for the transfer hydrogenation of ketones to alcohols in isopropanol as solvent and hydrogen source, salts 5–8 showed moderate activities for the transformation of acetophenone to 1-phenyl alcohol.

Four-component, one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles bearing 1-(2-phenylselenocyclohexyl) group

An efficient, one-pot, three-step, regioselective synthesis of 4-substituted 1-(2-phenylselenocyclohexyl)-1,2,3-triazoles, involving in situ generation of l-azido-2-phenylselenocyclohexane has been developed via four-component reaction of phenylselenenyl

Preparation method and application of propyne aryl ether compound

The invention particularly relates to a method for preparing propyne aryl ether compounds from aryl phenol, halogenated propyne and derivatives of the halogenated propyne, and belongs to the technical field of preparation of the propyne aryl ether compoun

Azoacetylenes for the Synthesis of Arylazotriazole Photoswitches

We report a modular approach toward novel arylazotriazole photoswitches and their photophysical characterization. Addition of lithiated TIPS-acetylene to aryldiazonium tetrafluoroborate salts gives a wide range of azoacetylenes, constituting an underexplored class of stable intermediates.In situdesilylation transiently leads to terminal arylazoacetylenes that undergo copper-catalyzed cycloadditions (CuAAC) with a diverse collection of organoazides. These include complex molecules derived from natural products or drugs, such as colchicine, taxol, tamiflu, and arachidonic acid. The arylazotriazoles display near-quantitative photoisomerization and long thermalZ-half-lives. Using the method, we introduce for the first time the design and synthesis of a diacetylene platform. It permits implementation of consecutive and diversity-oriented approaches linking two different conjugants to independently addressable acetylenes within a common photoswitchable azotriazole. This is showcased in the synthesis of several photoswitchable conjugates, with potential applications as photoPROTACs and biotin conjugates.