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2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91852-63-0 Structure
  • Basic information

    1. Product Name: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride
    2. Synonyms: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride
    3. CAS NO:91852-63-0
    4. Molecular Formula: C12H11Cl3O2
    5. Molecular Weight: 293.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91852-63-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride(91852-63-0)
    11. EPA Substance Registry System: 2,2-Dichloro-1-(4-ethoxyphenyl)cyclopropanecarbonyl chloride(91852-63-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 91852-63-0(Hazardous Substances Data)

91852-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91852-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,5 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91852-63:
(7*9)+(6*1)+(5*8)+(4*5)+(3*2)+(2*6)+(1*3)=150
150 % 10 = 0
So 91852-63-0 is a valid CAS Registry Number.

91852-63-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropane-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1-p-Ethoxyphenyl-2,2-dichlorocyclopropane-1-carbonyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91852-63-0 SDS

91852-63-0Relevant 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

Sun, Na-Bo,Jin, Jian-Zhong,Xu, Hui-Ying,Ke, Wei

, p. 4064 - 4066 (2013/05/08)

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 and biological activities of 2,2-dichloro-1-(4-ethoxyphenyl)-n- substituted phenyl cyclopropanecarboxamide

Sun, Na-Bo,Lei, Chao,Jin, Jian-Zhong,Ke, Wei

, p. 4071 - 4073 (2013/05/09)

Some new amide-type compounds are synthesized from 1-(4-ethyoxyphenyl)-2,2- dichlorocyclopropane-1-carboxylic acid and substituted anilline. Their structures were confirmed by 1H NMR, MS and elemental analysis. The bioassay results indicated that they sho

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

Sun, Na-Bo,Jin, Jian-Zhong,Lei, Chao,Ke, Wei

, p. 4067 - 4070 (2013/05/09)

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

Highly regioselective Friedel-Crafts reactions of electron-rich aromatic compounds with pyruvate catalyzed by Lewis acid-base: Efficient synthesis of pesticide cycloprothrin

Si, Yu-Gui,Chen, Jun,Li, Fan,Li, Jin-Hua,Qin, Ye-Jun,Jiang, Biao

, p. 898 - 904 (2007/10/03)

An efficient synthesis of aromatic lactate esters is reported via highly regioselective Friedel-Crafts reactions of electron-rich aromatic compounds with pyruvate ester promoted by TiCl4 in the presence of basic Al 2O3. The utility of the reaction is shown by the efficient synthesis of the pesticide cycloprothrin in high yield.

Investigation of Readily Available Chiral Compounds for Preparative Scale Resolutions

Duke, Colin C.,Wells, Robert J.

, p. 1641 - 1654 (2007/10/02)

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.

Insecticidal esters

-

, (2008/06/13)

The (+), (-) and (±) forms of the compounds of formula I STR1 wherein R1 is hydrogen or a methoxy, ethoxy, propoxy, methylthio, ethylthio, propylthio, fluoro, chloro, bromo, methyl, ethyl, nitro or amino group, and R2 is a hydrogen o

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