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539147

Ethyl chlorofluoroacetate

98%

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About This Item

Linear Formula:
Cl(F)CHCO2C2H5
CAS Number:
401-56-9
Molecular Weight:
140.54
NACRES:
NA.22
PubChem Substance ID:
24878381
UNSPSC Code:
12352100
EC Number:
206-930-5
MDL number:
MFCD00039333
Assay:
98%
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Quality Level

100

assay

98%

refractive index

n20/D 1.396 (lit.)

bp

133 °C (lit.)

density

1.212 g/mL at 25 °C (lit.)

functional group

chloro, ester, fluoro

SMILES string

CCOC(=O)C(F)Cl

InChI

1S/C4H6ClFO2/c1-2-8-4(7)3(5)6/h3H,2H2,1H3

InChI key

WUHVJSONZHSDFC-UHFFFAOYSA-N

Application

Ethyl chlorofluoroacetate may be used in the synthesis of:
  • chlorofluoroacetamide
  • ethyl α-fluoro silyl enol ether
  • chlorofluoroacetyl chloride

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

125.0 °F - closed cup

flash_point_c

51.67 °C - closed cup

ppe

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP0380
MKCD0678
MKBP6299V
MKBB4044
MKAA2927

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Xiao-Ting Huang et al.
The Journal of organic chemistry, 67(10), 3231-3234 (2002-05-11)
Ethyl alpha-fluoro silyl enol ether is stereoselectively synthesized in high yield from inexpensive chlorofluoroacetate and Mg (or Zn) in DMF (or HMPA). Lewis acid promoted aldol reaction of this enol ether with aldehydes and ketones gives alpha-fluoro-beta-hydroxy esters in good
One-step method for converting esters to acyl chlorides.
Middleton WJ.
The Journal of Organic Chemistry, 44(13), 2291-2292 (1979)
The preparation of some derivatives of chlorofluoroacetic acid.
Young JA and Tarrant P.
Journal of the American Chemical Society, 71(1), 3278-3285 (1949)

Global Trade Item Number

SKUGTIN
539147-25G04061836685881