41755-76-4

Basic information

• Product Name: 2-PHENOXYBENZOIC ACID ETHYL ESTER
• Synonyms: 2-PHENOXYBENZOIC ACID ETHYL ESTER;RARECHEM AL BI 1507;ethyl 2-phenoxybenzoate
• CAS NO: 41755-76-4
• Molecular Formula: C₁₅H₁₄O₃
• Molecular Weight: 242.27
• Mol File: 41755-76-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 143 °C
• Flash Point: 138.8°C
• Appearance: /
• Density: 1.129g/cm³
• Vapor Pressure: 0.000118mmHg at 25°C
• Refractive Index: 1.557
• CAS DataBase Reference: 2-PHENOXYBENZOIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENOXYBENZOIC ACID ETHYL ESTER(41755-76-4)
• EPA Substance Registry System: 2-PHENOXYBENZOIC ACID ETHYL ESTER(41755-76-4)

Safety Data

• Hazardous Substances Data: 41755-76-4(Hazardous Substances Data)

Usage

General Description

2-Phenoxybenzoic acid ethyl ester, also known as ethyl 2-phenoxybenzoate, is a chemical compound with the molecular formula C15H14O3. It is an ester formed from the condensation of 2-phenoxybenzoic acid and ethanol. 2-PHENOXYBENZOIC ACID ETHYL ESTER is commonly used as a flavor and fragrance ingredient, as well as a repellent for insects and pests. It is also used as an intermediate in the production of various other chemicals and substances. Additionally, it has applications in the pharmaceutical and cosmetic industries, making it a versatile compound with various uses.

InChI:InChI=1/C15H14O3/c1-2-17-15(16)13-10-6-7-11-14(13)18-12-8-4-3-5-9-12/h3-11H,2H2,1H3

Upstream product

• 64-17-5 ethanol 
• 2243-42-7 2-phenoxybenzoic acid 
• 144-55-8 sodium hydrogencarbonate 

Downstream Products

• 72084-13-0 2-phenoxybenzamide 
• 43038-37-5 2-phenoxybenzoic acid hydrazide 
• 13807-84-6 (2-phenoxyphenyl)methanol 
• 5888-53-9 2-phenoxybenzyl chloride 
• 25562-98-5 2-phenoxybenzyl cyanide 
• 25563-02-4 2-(2-phenoxyphenyl)acetic 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 

Relevant articles and documents

Selective Methylation of Arenes: A Radical C?H Functionalization/Cross-Coupling Sequence

A selective, nonchelation-assisted methylation of arenes has been developed. The overall transformation, which combines a C?H functionalization reaction with a nickel-catalyzed cross-coupling, offers rapid access to methylated arenes with high para selectivity. The reaction is amenable to late-stage methylation of small-molecule pharmaceuticals.

Alkoxyiminoacetamide derivatives and their use as fungicides

A fungicidal composition for agricultural use, which comprises a compound of the formula: STR1 wherein R1 and R2 are each hydrogen, lower alkyl or cyclo(lower)alkyl; R3 is lower alkyl or cyclo(lower)alkyl; R4 and R5 are each hydrogen, lower alkyl, lower alkoxy, halogen-substituted lower alkyl, lower alkyl-substituted silyl, halogen or nitro; A represents an unsaturated hydrocarbon group, a halogen-substituted unsaturated hydrocarbon group, a phenyl group or a heterocyclic group, among which the phenyl group and the heterocyclic group may be optionally substituted with not more than three substituents; and Z is --CH2 --, --CH(OH)--, --CO--, --O--, --S--, --NR-- (R being hydrogen or lower alkyl), --CH2 CH2 --, --CH=CH--, --CH2 O--, --CH2 S--, --CH2 SO--, --OCH2 --, --SCH2 -- or --SOCH2 --. STR2