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Merck
CN

35820

Ethyl dichloroacetate

≥99.0% (GC)

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About This Item

Linear Formula:
Cl2CHCOOC2H5
CAS Number:
535-15-9
Molecular Weight:
157.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57649426
EC Number:
208-611-6
Beilstein/REAXYS Number:
773995
MDL number:
MFCD00018858
Assay:
≥99.0% (GC)

Key Documents

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InChI key

IWYBVQLPTCMVFO-UHFFFAOYSA-N

InChI

1S/C4H6Cl2O2/c1-2-8-4(7)3(5)6/h3H,2H2,1H3

SMILES string

CCOC(=O)C(Cl)Cl

assay

≥99.0% (GC)

refractive index

n20/D 1.438

bp

54-55 °C/11 mmHg (lit.)

density

1.28 g/mL at 20 °C (lit.)

functional group

chloro, ester

Quality Level

100

Related Categories

General description

Ethyl dichloroacetate is an ester and its base catalyzed hydrolysis has been reported.

Application

Ethyl dichloroacetate may be used in the synthesis of α-halo-carboxylic acid ester.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Eye Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCM1641
BCCK4378
BCCD5719
BCCB9768
BCBZ2955

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General Base Catalysis of Ester Hydrolysis1.
Jencks WP and Carriuolo J.
Journal of the American Chemical Society, 83(7), 1743-1750 (1961)
Reaction of B-alkyl-9-borabicyclo [3.3. 1] nonanes with ethyl mono-and dihaloacetates under the influence of potassium tert-butoxide. A convenient procedure for the conversion of olefins into esters or. alpha.-halo esters via hydroboration.
Brown HC and Milorad M. Rogic.
Journal of the American Chemical Society, 91(8), 2146-2147 (1969)

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