452114
Ethyl bromofluoroacetate
97%
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About This Item
Linear Formula:
BrCH(F)CO2C2H5
CAS Number:
Molecular Weight:
184.99
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-928-4
MDL number:
Assay:
97%
InChI key
ULNDTPIRBQGESN-UHFFFAOYSA-N
InChI
1S/C4H6BrFO2/c1-2-8-4(7)3(5)6/h3H,2H2,1H3
SMILES string
CCOC(=O)C(F)Br
assay
97%
refractive index
n20/D 1.424 (lit.)
bp
154 °C (lit.)
density
1.565 g/mL at 25 °C (lit.)
storage temp.
2-8°C
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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R Ocampo et al.
The Journal of organic chemistry, 67(1), 72-78 (2002-01-05)
The presence of catalytic amounts of CeCl(3) improves yields and simplifies procedure in the Reformatsky reactions of ethyl bromofluoroacetate with aldehydes and ketones to generate diastereomeric mixtures of alpha-fluoro-beta-hydroxy esters, some of which can be separated by crystallization or column
Journal of Fluorine Chemistry, 77, 45-45 (1996)
Synthesis of (E)-and (Z)-fluoro-olefin analogues of potent dipeptidyl peptidase IV inhibitors.
Van der Veken P, et al.
Tetrahedron Letters, 44(33), 6231-6234 (2003)
Journal of the Chemical Society. Perkin Transactions 1, 49-49 (1991)
Thibault Ferrary et al.
Organic letters, 15(21), 5598-5601 (2013-10-22)
The synthesis of highly functionalized monofluorinated cyclopropanes based on a Michael Initiated Ring Closure (MIRC) reaction has been developed. The addition of quaternary ammonium salts derived from ethyl bromofluoroacetate on a panel of electron deficient alkenes followed by cyclization gave
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