25562-98-5

Basic information

• Product Name: 2-PHENOXYPHENYLACETONITRILE
• Synonyms: 2-(2-PHENOXYPHENYL)ACETONITRILE;2-PHENOXYPHENYLACETONITRILE;2-Phenoxybenzyl cyanide;2-[2-(phenoxy)phenyl]ethanenitrile;2-Phenoxybenzyl cyanide, 2-(Cyanomethyl)diphenyl ether
• CAS NO: 25562-98-5
• Molecular Formula: C₁₄H₁₁NO
• Molecular Weight: 209.24
• Product Categories: Aromatic Nitriles
• Mol File: 25562-98-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 145°C 1mm
• Flash Point: 145°C/1mm
• Appearance: /
• Density: 1,11 g/cm3
• Vapor Pressure: 0.000101mmHg at 25°C
• Refractive Index: 1.577
• BRN: 2727468
• CAS DataBase Reference: 2-PHENOXYPHENYLACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENOXYPHENYLACETONITRILE(25562-98-5)
• EPA Substance Registry System: 2-PHENOXYPHENYLACETONITRILE(25562-98-5)

Safety Data

• Hazard Codes: Xi
• Statements: R22:Harmful if swallowed.
• Safety Statements: S36/37:Wear suitable protective clothing and gloves.
• RIDADR: 3276
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 25562-98-5(Hazardous Substances Data)

Usage

General Description

2-Phenoxyphenylacetonitrile is a chemical compound that falls under the category of phenylpropanoids and polyketides. 2-PHENOXYPHENYLACETONITRILE exists as a solid and is commonly used in industrial processes. It can be synthesized through various processes, and after synthesis, it typically appears as a pale-yellow to light-brown low-melting crystalline solid. As with many chemical substances, necessary precautions should be taken while handling 2-Phenoxyphenylacetonitrile to avoid any potential health risks or hazards. In-depth knowledge about this chemical is vital to ensure its safe and effective usage. For more specific information about the chemical properties and potential applications of 2-Phenoxyphenylacetonitrile, one should refer to scientific literature or material safety data sheets (MSDS).

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

Upstream product

• 108-95-2 phenol 
• 446-52-6 2-Fluorobenzaldehyde 
• 773837-37-9 sodium cyanide 
• 5888-53-9 2-phenoxybenzyl chloride 
• 41755-76-4 ethyl 2-phenoxybenzoate 
• 88-67-5 2-Iodobenzoic acid 
• 108-90-7 chlorobenzene 
• 33838-32-3 potassium 2-formylphenolate 
• 19434-34-5 2-(phenoxy)benzaldehyde 
• 2243-42-7 2-phenoxybenzoic acid 
• 13807-84-6 (2-phenoxyphenyl)methanol 
• 143-33-9 sodium cyanide 

Downstream Products

• 53921-70-3 dibenzo[b,f]oxepine-10-carboxylic acid 
• 1580001-09-7 5-(2-phenoxybenzyl)-2H-1,2,4-triazole-3(4H)-thione 
• 1580001-12-2 5-(2-phenoxybenzyl)-3-methylthio-4H-1,2,4-triazole 
• 1580001-14-4 5-(2-phenoxybenzyl)-3-ethylthio-4H-1,2,4-triazole 
• 1580001-15-5 5-(2-phenoxybenzyl)-3-propylthio-4H-1,2,4-triazole 
• 1580001-16-6 5-(2-phenoxybenzyl)-3-benzylthio-4H-1,2,4-triazole 
• 1417512-55-0 ethyl 2-(2-phenoxyphenyl)acetate 
• 159731-09-6 2-(2-phenoxyphenyl)acetic acid hydrazide 
• 1580001-29-1 2-amino-5-(2-phenoxybenzyl)-1,3,4-oxadiazole 
• 1580001-32-6 5-ethoxy-3-(2-phenoxybenzyl)-4H-1,2,4-triazole 
• 128039-27-0 5-(p-methoxyphenyl)benzoxepine 
• 144836-66-8 5-bromo-6-(p-methoxyphenyl)dibenzoxepine 

Relevant articles and documents

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

Provided in the present invention are a heterocyclic compound and an organic light emitting device comprising the same. Provided in the present invention is a heterocyclic compound presented by following chemical formula 1. The heterocyclic compound according to embodiments of the present invention has a proper energy level, and has excellent electrochemical stability and thermal stability. Therefore, an organic light emitting device including the compound provides high efficiency and/or high driving stability.

Synthesis, receptor affinity and effect on pentylenetetrazole-induced seizure threshold of novel benzodiazepine analogues: 3-Substituted 5-(2-phenoxybenzyl)-4H-1,2,4-triazoles and 2-amino-5-(phenoxybenzyl)-1,3,4- oxadiazoles

The new series of 5-(2-phenoxybenzyl)-4H-1,2,4-triazoles, possessing C-3 thio, alkylthio and ethoxy substituents, and 2-amino-5-(2-phenoxybenzyl)-1,3,4- oxadiazoles were designed and synthesized as novel benzodiazepine analogues. Most of them revealed sim

Substituted (2-Phenoxyphenyl)acetic Acids with Antiinflammatory Activity. 1

The synthesis and antiinflammatory activity of a series of substituted (2-phenoxyphenyl)acetic acids are described.Initial screening in the adjuvant arthritis test showed that halogen substitution in the phenoxy ring enhanced activity considerably.Ulcerogenic potential, as measured by the minimum ulcerogenic dose (MUD), was low in almost all the acids tested. acetic acid possessed the most favorable combination of potency with low toxicity, including ulcerogenicity, and this compound is now in therapeutic use.