41755-76-4

Usage

Uses

Used in Flavor and Fragrance Industry:
2-Phenoxybenzoic acid ethyl ester is used as a flavor and fragrance ingredient due to its aromatic properties, enhancing the sensory experience of various products.
Used as Insect and Pest Repellent:
In the agricultural and household sectors, 2-Phenoxybenzoic acid ethyl ester serves as an effective repellent for insects and pests, protecting crops and living spaces from unwanted infestations.
Used as an Intermediate in Chemical Production:
2-Phenoxybenzoic acid ethyl ester is utilized as an intermediate in the synthesis of various other chemicals and substances, contributing to the development of a wide range of products.
Used in Pharmaceutical Industry:
Within the pharmaceutical sector, 2-Phenoxybenzoic acid ethyl ester is employed for its potential applications in drug development and formulation, benefiting from its chemical properties.
Used in Cosmetic Industry:
In the cosmetic industry, 2-Phenoxybenzoic acid ethyl ester is used in the creation of skincare and beauty products, capitalizing on its versatility and compatibility with various formulations.

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 academic research and scientific papers

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.

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

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