ETHYL 3-CHLOROBENZOATE

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Products Intro: Product Name:ETHYL 3-CHLOROBENZOATE
CAS:1128-76-3
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CAS:1128-76-3
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CAS:1128-76-3
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Products Intro: Product Name:ETHYL 3-CHLOROBENZOATE
CAS:1128-76-3
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Products Intro: Product Name:Ethyl 3-chlorobenzoate
CAS:1128-76-3
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-27073

ETHYL 3-CHLOROBENZOATE manufacturers

ETHYL 3-CHLOROBENZOATE Basic information
Product Name:ETHYL 3-CHLOROBENZOATE
Synonyms:Benzoic acid, m-chloro-, ethyl ester;Ethyl m-chlorobenzoate;ETHYL 3-CHLOROBENZOATE;3-CHLOROBENZOIC ACID ETHYL ESTER;NSC 67339;RARECHEM AL BI 0056;Ethyl 3-chlorobenzoate, 98+%;Ethyl 3-Chlorobenzoate >
CAS:1128-76-3
MF:C9H9ClO2
MW:184.62
EINECS:214-441-3
Product Categories:Aromatic Esters;Benzoic acid;Acids & Esters;Chlorine Compounds
Mol File:1128-76-3.mol
ETHYL 3-CHLOROBENZOATE Structure
ETHYL 3-CHLOROBENZOATE Chemical Properties
Boiling point 118-120°C 13mm
density 1,186 g/cm3
refractive index 1.5220
Fp 118-120°C/13mm
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow
BRN 2045877
CAS DataBase Reference1128-76-3(CAS DataBase Reference)
EPA Substance Registry SystemBenzoic acid, 3-chloro-, ethyl ester (1128-76-3)
Safety Information
Safety Statements 24/25
HS Code 2916399090
MSDS Information
ProviderLanguage
ALFA English
ETHYL 3-CHLOROBENZOATE Usage And Synthesis
Synthesis
CHLOROETHANE

75-00-3

3-Chlorobenzoic acid

535-80-8

ETHYL 3-CHLOROBENZOATE

1128-76-3

Under stirring conditions, 3-chlorobenzoic acid (1.00 mmol), chloroethane (1.20 mmol), and IL-1 (0.30 mmol) were sequentially added to a two-necked flask containing 6 mL of 50% aqueous ethanol solution. Subsequently, the temperature of the reaction system was raised to 70 °C and maintained at this temperature in a water bath. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reactor was cooled to room temperature. The reaction mixture was diluted with 10 mL of water and extracted with ethyl acetate (3 x 5 mL). The organic phases were combined, dried over anhydrous Na2SO4 and filtered, and the filtrate was concentrated in a rotary evaporator to give ethyl m-chlorobenzoate. The catalyst was dried under vacuum at 80 °C for 6 h after removing the solvent and could be recycled for the next round of reaction. All esterification products need to be further purified by column chromatography.

References[1] Catalysis Letters, 2017, vol. 147, # 11, p. 2764 - 2771
ETHYL 3-CHLOROBENZOATE Preparation Products And Raw materials
Raw materials3-BROMOCHLOROBENZENE-->Ethanol-->CHLOROETHANE-->3-Chlorobenzoic acid-->3-Chlorobenzaldehyde-->Ethyl formate-->Water
Preparation Products3-CHLOROPHENACYL BROMIDE
Tag:ETHYL 3-CHLOROBENZOATE(1128-76-3) Related Product Information
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