717-30-6

Basic information

• Product Name: Ethyl 2-(2,4-difluorophenoxy)acetate
• Synonyms: Ethyl 2-(2,4-difluorophenoxy)acetate;methyl 2-(2,4-difluorophenoxy)acetate;(2,4-DIFLUOROPHENOXY)-ACETIC ACID ETHYL ESTER
• CAS NO: 717-30-6
• Molecular Formula: C₁₀H₁₀F₂O₃
• Molecular Weight: 216.1814064
• EINECS: -0
• Mol File: 717-30-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethyl 2-(2,4-difluorophenoxy)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2-(2,4-difluorophenoxy)acetate(717-30-6)
• EPA Substance Registry System: Ethyl 2-(2,4-difluorophenoxy)acetate(717-30-6)

Safety Data

• Hazardous Substances Data: 717-30-6(Hazardous Substances Data)

Upstream product

• 367-27-1 2,4-difluorophenol 
• 105-36-2 ethyl bromoacetate 
• 105-39-5 chloroacetic acid ethyl ester 

Downstream Products

• 713-12-2 <2,4-Difluor-phenoxy>-acethydroxamsaeure 
• 399-44-0 2-(2,4-difluorophenoxy)acetic acid 
• 399-42-8 (2,4-difluoro-phenoxy)-acetyl chloride 
• 826990-50-5 [(2,4-difluorophenoxyacetyl)(cyano)methylene]triphenylphosphorane 
• 826990-56-1 [(2,4-difluorophenoxyacetyl)(ethoxycarbonyl)methylene]triphenylphosphorane 
• 1280218-22-5 6-(2,4-difluorophenoxy)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-40-7 6-(2,4-difluorophenoxy)-2-methylsulfanyl-8-(tetrahydrothiopyran-4-yl)-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-31-6 6-(2,4-difluorophenoxy)-8-(3-hydroxypropyl)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-33-8 6-(2,4-difluorophenoxy)-2-methylsulfanyl-8-(2-methylsulfanylethyl)-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1313610-16-0 6-(2,4-difluorophenoxy)-2-methanesulfonyl-8-(2-methanesulfonylethyl)-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-08-7 6-(2,4-difluorophenoxy)-8-(2-methanesulfonylethyl)-2-(tetrahydropyran-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-35-0 6-(2,4-difluorophenoxy)-2-methylsulfanyl-8-(3-methylsulfanylpropyl)-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-36-1 6-(2,4-difluorophenoxy)-2-methanesulfonyl-8-(3-methanesulfonylpropyl)-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1280218-09-8 6-(2,4-difluorophenoxy)-8-(3-methanesulfonylpropyl)-2-(tetrahydropyran-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one 

Relevant articles and documents

Inhibitor containing fused ring derivative as well as preparation method and application thereof

The invention relates to an inhibitor containing fused ring derivative as well as a preparation method and application thereof. Particularly, the invention relates to a compound as shown in a generalformula (I), a preparation method thereof, a pharmaceuti

Synthesis and larvicidal activity of 1,3,4-oxadiazole derivatives containing a 3-chloropyridin-2-yl-1H-pyrazole scaffold

Abstract: A new series of 1,3,4-oxadiazole derivatives with a 3-chloropyridin-2-yl-1H-pyrazole moiety was designed, synthesized, and characterized. The results of bioassay against Helicoverpa armigera and Plutella xylostella indicated that some of the synthesized compounds showed remarkable larvicidal activity. In particular, the LC50 values of the most active compounds against P. xylostella were 46.5, 23.9, and 13.9?mg/dm3, and against Helicoverpa armigera were 88.3 and 69.5?mg/dm3, the latter being slightly better than commercial chlorpyrifos (LC50 103.77?mg/dm3). Preliminary SAR was also discussed. Graphical abstract: [Figure not available: see fulltext.].

Synthesis and biological activity of 1-(Substituted phenoxyacetoxy)- 1-(pyridin-2-yl or thien-2-yl)methylphosphonates

A series of novel O,O-dimethyl 1-(substituted phenoxyacetoxy)-1-(pyridin-2-yl or thien-2-yl)methylphosphonates 6a-n and 7a-d were synthesized. Their structures were confirmed by IR, 1H NMR, mass spectroscopy, and elemental analyses. The results of preliminary bioassays show that some of the title compounds exhibit moderate to good herbicidal and fungicidal activities. For example, the title compounds 6a, 6c, 6l, 6m, and 7d possess 90-100% inhibition against most of the tested plants at the dosage of 1500 g ai/ha, whereas the title compounds 6b, 6g-h and 6n possess 92-100% inhibition against Fusarium oxysporum, Phyricularia grisea, Botrytis cinereapers, Gibberella zeae, Sclerotinia sclerotiorum, and Cercospora beticola at the concentration of 50mg/L.