60758-84-1

Basic information

• Product Name: 4-PROPOXYBENZONITRILE
• Synonyms: P-PROPOXYBENZONITRILE;4-PROPYLOXYBENZONITRILE;4-PROPOXYBENZONITRILE;4-N-PROPYLOXYBENZONITRILE;4-n-Propoxybenzonitrile
• CAS NO: 60758-84-1
• Molecular Formula: C₁₀H₁₁NO
• Molecular Weight: 161.2
• Product Categories: Aromatic Nitriles
• Mol File: 60758-84-1.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 280.2 °C at 760 mmHg
• Flash Point: 117.7 °C
• Appearance: /
• Density: 1.03 g/cm³
• Vapor Pressure: 0.00385mmHg at 25°C
• Refractive Index: 1.515
• CAS DataBase Reference: 4-PROPOXYBENZONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-PROPOXYBENZONITRILE(60758-84-1)
• EPA Substance Registry System: 4-PROPOXYBENZONITRILE(60758-84-1)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-22
• Safety Statements: 36/37
• RIDADR: 3439
• Hazardous Substances Data: 60758-84-1(Hazardous Substances Data)

Usage

General Description

4-Propoxybenzonitrile is a chemical compound with the molecular formula C10H9NO. It is an organic nitrile with a propoxy (C3H7O) group attached to a benzene ring. 4-propoxybenzonitrile is commonly used as an intermediate in the manufacture of pharmaceuticals and agrochemicals. It is also used in the synthesis of other organic compounds and as a key building block for organic chemistry research. 4-Propoxybenzonitrile is a colorless to light yellow liquid with a faint odor, and it is considered to be moderately hazardous if ingested, inhaled, or absorbed through the skin. It is important to handle this chemical with care and follow proper safety protocols when working with it.

InChI:InChI=1/C10H11NO/c1-2-7-12-10-5-3-9(8-11)4-6-10/h3-6H,2,7H2,1H3

Upstream product

• 767-00-0 4-cyanophenol 
• 106-94-5 propyl bromide 
• 107-08-4 1-iodo-propane 
• 33148-47-9 4-allyloxy-benzonitrile 
• 52805-36-4 4-benzyloxybenzonitrile 
• 71-23-8 propan-1-ol 
• 623-03-0 4-Cyanochlorobenzene 
• 623-00-7 4-bromobenzenecarbonitrile 
• 3328-57-2 sodium 4-cyanophenolate 
• 80122-67-4 1-propoxy-4-vinylbenzene 

Downstream Products

• 3540-94-1 propoxy-4 benzimidate d'ethyle 
• 767-00-0 4-cyanophenol 
• 138631-06-8 5-[5-(4-Propoxy-phenyl)-tetrazol-2-yl]-pentanenitrile 
• 138631-04-6 5-(4-propoxyphenyl)-2-<4-(1H-tetrazol-5-yl)butyl>-2H-tetrazole 
• 145259-49-0 N-hydroxy-4-propoxybenzamidine 
• 1380593-07-6 (Z)-5-(4-methoxybenzylidene)-2-(4-propoxyphenyl)-5H-thiazol-4-one 
• 90925-43-2 4-n-propyloxybenzyl alcohol 
• 21244-33-7 1-(4-propoxyphenyl)methanamine 
• 125575-11-3 C₂₃H₁₆O₆*C₁₆H₂₇N₃O 
• 125575-15-7 dichlorure de N-<(methylenedioxy-3,4 benzyl)-4 piperazinyl-1> propoxy-4 benzamidinium 
• 125575-14-6 N-(3-Dimethylamino-propyl)-4-propoxy-benzamidine; hydrochloride 
• 125575-13-5 N-[2-(4-Benzo[1,3]dioxol-5-ylmethyl-piperazin-1-yl)-ethyl]-4-propoxy-benzamidine; hydrochloride 
• 135420-40-5 N-(2-Diethylamino-ethyl)-4-propoxy-benzamidine; hydrochloride 

Relevant articles and documents

Discovery and characterization of a novel perylenephotoreductant for the activation of aryl halides

To develop a photocatalyst with catalytical activity for substrates with low reactivities is always highly desired. Herein, based on the principle of structure–property relationships, we rationally designed the natural product cercosporin, the naturally occurring perylenequinonoid pigment, to develop a novel organic perylenephotoreductant, hexacetyl reduced cercosporin (HARCP), through structural manipulation. Compared with cercosporin, HARCP shows prominent electrochemical and photophysical characteristics with greatly improved photoreductive activity, fluorescence lifetime and fluorescence quantum yield. These properties allowed HARCP as a powerful photoreductant to efficiently realize a series of benchmark reactions, including photoreduction, alkoxylation and hydroxylation to construct C–H and C–O bonds using aryl halides as substrates under mild conditions, all of which have never been achieved by the same photocatalyst. Thus, this study well supports the notion that the principle between structural manipulation and photocatalytic activity is of great significance to design customized photocatalysts for photoredox chemistry.

Preparation method of nitrile compound

The present invention belongs to the field of organic synthesis technology, specifically relates to a method for preparing a nitrile compound, aldehyde oxime derivatives as raw materials, adding DPPA and DBU, reacting in an organic solvent, one step to pr

Cobalt-containing mesoporous ZSM-5 zeolite catalyzed C=C bond cleavage of alkenes to form nitriles

Cobalt-containing mesoporous ZSM-5 zeolite (Co-ZSM-5-M) catalyst showed high catalytic activity, selectivity, and excellent reusability in C=C double-bond cleavage of alkenes to form aromatic nitriles. All reactions proceeded smoothly to afford the desired target products in moderate to high yields under the optimal conditions. The Co-ZSM-5-M catalyst was recycled up to at least seven consecutive cycles without significant loss of its catalytic performance.