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Fórmula lineal:
C6F5COCl
Número CAS:
Peso molecular:
230.52
EC Number:
218-842-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2054397
MDL number:
refractive index
n20/D 1.453 (lit.)
bp
158-159 °C (lit.)
density
1.601 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
Fc1c(F)c(F)c(c(F)c1F)C(Cl)=O
InChI
1S/C7ClF5O/c8-7(14)1-2(9)4(11)6(13)5(12)3(1)10
InChI key
MYHOHFDYWMPGJY-UHFFFAOYSA-N
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P Falardeau et al.
Analytical biochemistry, 208(2), 311-316 (1993-02-01)
We describe a method for quantifying diacylglycerols as their 1-pentafluorobenzoyl-2-acyl-3-acetyl-glycerol derivatives by capillary gas chromatography-negative ion chemical ionization-mass spectrometry. The basis of the method resides in the sequential treatment of diacylglycerols with acetic anhydride, pancreatic lipase, and pentafluorobenzoyl chloride. Cultured
Sören Jensen et al.
Journal of agricultural and food chemistry, 57(13), 5872-5877 (2009-06-06)
A method was developed for the extraction of lipids and analysis of halogenated phenols and alkylphenols in marine organisms. The extraction efficiency was evaluated by comparing the extractable lipid content and the recovery of 13 added phenols from three different
W C Hubbard et al.
Analytical biochemistry, 236(2), 309-321 (1996-05-01)
Investigation of the role of diacylglycerol molecular species in signal transduction in human basophils has been impeded by the lack of an assay method with adequate sensitivity and selectivity. Conversion of 1-stearoyl-2-arachidonoyl-sn-3-glycerol to the pentafluorobenzoyl ester conveys electron-capture properties to