91852-63-0

Basic information

• Product Name: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride
• Synonyms: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride
• CAS NO: 91852-63-0
• Molecular Formula: C₁₂H₁₁Cl₃O₂
• Molecular Weight: 293.57
• Mol File: 91852-63-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride(91852-63-0)
• EPA Substance Registry System: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride(91852-63-0)

Safety Data

• Hazardous Substances Data: 91852-63-0(Hazardous Substances Data)

Upstream product

• 97558-55-9 α-cyano-3-phenoxybenzyl radical 
• 104023-75-8 1-(4'-ethoxyphenyl)-2,2-dichlorocyclopropane-1-carboxylic acid 
• 103-73-1 Phenetole 
• 101492-41-5 1-(4-ethoxyphenyl)-2,2-dichlorocyclopropane-1-carboxylic acid methyl ester 
• 888498-57-5 methyl 2-(4-ethoxyphenyl)lactate 
• 928118-57-4 2-(4-ethoxy-phenyl)-acrylic acid methyl ester 

Downstream Products

• 84772-64-5 (S)-2,2-Dichloro-1-(4-ethoxy-phenyl)-cyclopropanecarboxylic acid (3aR,4R,6aR)-2,2-dimethyl-6-oxo-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 
• 84772-63-4 (R)-2,2-Dichloro-1-(4-ethoxy-phenyl)-cyclopropanecarboxylic acid (3aR,4R,6aR)-2,2-dimethyl-6-oxo-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 
• 1448178-31-1 1-(2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl)-3-phenylthiourea 
• 1448178-32-2 1-(2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl)-3-(4-methylphenyl)thiourea 
• 1448178-33-3 1-(2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl)-3-(3-methylphenyl)thiourea 
• 946086-44-8 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-2,3-dimethylpiperidin-1-yl ketone 
• 1449376-11-7 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-3,5-dimethylpiperidin-1-yl ketone 
• 946086-45-9 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-4-tertbutylpiperidin-1-yl ketone 
• 1449376-01-5 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-4-methylpiperidin-1-yl ketone 
• 1449376-03-7 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-3-methylpiperidin-1-yl ketone 
• 946086-43-7 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-2,6-dimethylpiperidin-1-yl ketone 
• 1449376-09-3 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanyl-3,3-dimethylpiperidin-1-yl ketone 
• 1162060-64-1 2,2-dichloro-1-(4-ethoxyphenyl)-N-(2,4-difluorophenyl)cyclopropane carboxamide 
• 1162060-61-8 2,2-dichloro-1-(4-ethoxyphenyl)-N-(4-nitrophenyl)-cyclopropane carboxamide 

Relevant articles and documents

Synthesis and biological activities of 3-1-(3-(2-chloro-3,3,3-trifluoro- prop-1-enyl- 2,2-dimethylcyclopropanecarbonyl)-3-substituted phenyl thiourea

Some thiourea compounds containing pyrethroids are synthesized. Their structures were confirmed by 1H NMR, MS and elemental analysis. The bioassay results indicated that they showed moderate insecticidal and fungicidal activity.

Synthesis, structure and biological activities of 2,2-dichloro-1-(4- ethoxyphenyl)-cyclopropanyl substituted piperidin-1-yl Ketone

Ten new amide-type compounds, which are pyrethroids containing piperidine, are synthesized from 1-(4-ethyoxyphenyl)-2,2- dichlorocyclopropane-1-carboxylic acid and substituted piperidine. Their structures were confirmed by 1H NMR, MS and elemen

Investigation of Readily Available Chiral Compounds for Preparative Scale Resolutions

Diastereoisomeric esters were formed by reaction of racemic carboxylic acids with the readily available hydroxy lactone derivatives, 2,3-O-isopropylidene-D(+)-ribono-1,4-lactone, D(-)-2-hydroxy-3,3-dimethylbutyro-1,4-lactone (D(-)-pantolactone) and 1,2-O-isopropylidene-(+)-a-D-glucofuranurono-6,3-lactone.In all cases separation of the diastereoisomeric esters was achieved by crystallization and/or chromatography.Purity of the diastereoisomers could be determined by h.p.l.c. or by 1H n.m.r.Hydrolysis under mild basic conditions followed by treatment with acid gave optically pure carboxylic acids.The facile separation by crystallization and/or chromatography of diastereoisomers prepared from racemic endo-1,4,5,6,7,7-hexachlorobicyclohept-5-ene-2-carboxylic acid suggested that the resolved acid may be useful as a resolving agent.This was shown by separation of diastereoisomers formed from the resolved acid and racemic 1-(3'-phenoxyphenyl)prop-2-yn-1-ol and racemic 1-cyano-1-(3'-phenoxyphenyl)methanol respectively.Optically pure 1-(3'-phenoxyphenyl)prop-2-yn-1-ol was obtained by hydrolysis of the separated diastereoisomers.