168971-54-8

Basic information

• Product Name: 2-(PHENOXYMETHYL)BENZONITRILE 97
• Synonyms: 2-(PHENOXYMETHYL)BENZONITRILE 97;2-(PHENOXYMETHYL)BENZONITRILE;2-(Phenoxymethyl)benzonitrile 97%
• CAS NO: 168971-54-8
• Molecular Formula: C₁₄H₁₁NO
• Molecular Weight: 209.24324
• Mol File: 168971-54-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 62-64
• Boiling Point: 349.3°C at 760 mmHg
• Flash Point: 147.4°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 4.74E-05mmHg at 25°C
• Refractive Index: 1.597
• CAS DataBase Reference: 2-(PHENOXYMETHYL)BENZONITRILE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(PHENOXYMETHYL)BENZONITRILE 97(168971-54-8)
• EPA Substance Registry System: 2-(PHENOXYMETHYL)BENZONITRILE 97(168971-54-8)

Safety Data

• Hazard Codes: Harmful:
• Hazardous Substances Data: 168971-54-8(Hazardous Substances Data)

Usage

General Description

2-(PhenoxyMethyl)Benzonitrile 97 is a chemical compound that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a clear, colorless liquid with a molecular formula of C14H11NO and a molecular weight of 209.25. The compound is known for its high level of purity, with a 97% minimum assay, making it suitable for use in a wide range of research and industrial applications. It is important to handle this chemical with caution, as it may cause skin and eye irritation upon contact. Overall, 2-(PhenoxyMethyl)Benzonitrile 97 is an important chemical used in various industries for its versatile applications.

InChI:InChI=1/C14H11NO/c15-10-12-6-4-5-7-13(12)11-16-14-8-2-1-3-9-14/h1-9H,11H2

Upstream product

• 612-13-5 2-cyanobenzyl chloride 
• 108-95-2 phenol 
• 7468-67-9 o-formylbenzonitrile 
• 22115-41-9 2-(bromomethyl)benzonitrile 

Downstream Products

• 168971-56-0 2-phenoxymethyl-benzylamine 

Relevant articles and documents

Preparation method of benzyl aryl ether and application of benzyl aryl ether in synthesis

and, 6-dihydrodibenzo [11 - b] oxazepine e -11 - ketone compounds are synthesized through a one-step reaction of benzaldehyde compounds and phenolic compounds through one-step reaction. The benzyl aryl ether and 6 and 11 -dihydrodibenzo [b, e] oxazepine -11 - ketone compound respectively have a chemical structure formula shown in a formula I and II. The invention discloses a synthesis method of the compound. Benzaldehyde compound After completion of the reaction, I, 6-dihydrodibenzo [11 - b] oxazepine e ketone compound -11 - can be synthesized through an oxidation or hydrolysis step and a ring closing step after the reaction is complete II.

Synthesis of 2-aryloxymethylbenzonitriles from 2-cyanobenzyl chloride

Fourteen 2-Aryloxymethylbenzonitriles were synthesized from 2-cyanobenzyl chloride and various substituted phenols with potassium carbonate as a base in N,N-dimethyl formamide at 80-110 °C in good to excellent yields. The products, 13 of which are new, we