3-(4-bromophenyl)-2-cyanoacrylic acid

Names

[ CAS No. ]:
339548-64-0

[ Name ]:
3-(4-bromophenyl)-2-cyanoacrylic acid

[Synonym ]:
(2E)-3-(4-Bromophenyl)-2-cyanoacrylic acid
2-Propenoic acid, 3-(4-bromophenyl)-2-cyano-, (2E)-
3-(4-BROMOPHENYL)-2-CYANO-2-PROPENOIC ACID
p-Bromobenzylidenecyanoacetic acid
MFCD07798953
BrCCA
p-Bromo-α-cyanocinnamic acid
4-Bromo-α-cyanocinnamic acid

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
395.4±32.0 °C at 760 mmHg

[ Molecular Formula ]:
C10H6BrNO2

[ Molecular Weight ]:
252.064

[ Flash Point ]:
192.9±25.1 °C

[ Exact Mass ]:
250.958176

[ LogP ]:
2.95

[ Vapour Pressure ]:
0.0±1.0 mmHg at 25°C

[ Index of Refraction ]:
1.661

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332-H315-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ RIDADR ]:
NONH for all modes of transport

Articles

4-Chloro-alpha-cyanocinnamic acid is an advanced, rationally designed MALDI matrix.

Proc. Natl. Acad. Sci. U. S. A. 105(34) , 12200-5, (2008)

Matrix-assisted laser desorption ionization (MALDI) has become an enabling technology for the fields of protein mass spectrometry (MS) and proteomics. Despite its widespread use, for example, in prote...

Ion yields in UV-MALDI mass spectrometry as a function of excitation laser wavelength and optical and physico-chemical properties of classical and halogen-substituted MALDI matrixes.

Anal. Chem. 84(15) , 6567-76, (2012)

The laser wavelength constitutes a key parameter in ultraviolet-matrix-assisted laser desorption ionization-mass spectrometry (UV-MALDI-MS). Optimal analytical results are only achieved at laser wavel...

The new matrix 4-chloro-alpha-cyanocinnamic acid allows the detection of phosphatidylethanolamine chloramines by MALDI-TOF mass spectrometry.

J. Am. Soc. Mass Spectrom. 20(5) , 867-74, (2009)

Phosphatidylethanolamines (PEs) are abundant lipid constituents of the cellular membrane. The amino group of PEs exhibits high reactivity with hypochlorous acid that is generated under inflammatory co...


More Articles

Related Compounds

  • (E)-3-(4-bromophenyl)-2-cyanoacrylic acid
  • (E)-3-(4-Bromophenyl)-2-cyanoacrylic acid
  • 3-(4-broMophenyl)-2-Methoxypropanoic acid
  • 3-(4-bromophenyl)-2-oxopropanoic acid
  • 3-(4-bromophenyl)-2-ethylacrylic acid
  • 3-(4-bromophenyl)-2-methylacrylic acid ethyl ester
  • N-(1-propionyl-1,2,3,4-tetrahydroquinolin-7-yl)-4-propylbenzenesulfonamide
  • 3-chloro-4-fluoro-N-(1-propionyl-1,2,3,4-tetrahydroquinolin-7-yl)benzenesulfonamide
  • N-[3-({[(1-cyano-1,2-dimethylpropyl)carbamoyl]methyl}amino)-4-methylphenyl]cyclopropanecarboxamide
  • 1-(4-chlorophenyl)-2-(isopropylthio)-5-(4-methoxyphenyl)-1H-imidazole
  • (4-(6-Chlorobenzo[d]thiazol-2-yl)piperazin-1-yl)(pyrazin-2-yl)methanone
  • 3-fluoro-N-[2-(pyridin-3-yl)-2-(1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzamide
  • N-(1-cyano-1-cyclopropylethyl)-2-[(3,4-dimethoxyphenyl)(methyl)amino]acetamide
  • Methyl 2-hydroxy-5-[(1-oxopropyl)amino]benzoate
  • 1-Cyclohexyl-3-(cyclohexylamino)pyrrolidine-2,5-dione
  • N-(4-ethoxybenzo[d]thiazol-2-yl)-2-(N-methylmethylsulfonamido)-N-(pyridin-2-ylmethyl)acetamide
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