407070
2-Chloro-4-(trifluoromethyl)pyrimidine
99%
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About This Item
Productos recomendados
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.447 (lit.)
bp
60 °C/10 mmHg (lit.)
density
1.513 g/mL at 25 °C (lit.)
functional group
chloro
fluoro
SMILES string
FC(F)(F)c1ccnc(Cl)n1
InChI
1S/C5H2ClF3N2/c6-4-10-2-1-3(11-4)5(7,8)9/h1-2H
InChI key
FZRBTBCCMVNZBD-UHFFFAOYSA-N
General description
2-Chloro-4-(trifluoromethyl)pyrimidine is a pyrimidine derivative. Its density and refractive index have been determined.
Application
2-Chloro-4-(trifluoromethyl)pyrimidine may be used to investigate the effect of chemical substitutions on the interfacial interactions of pyrimidines with the phospholipid-mimic immobilized-artificial-membrane (IAM) chromatographic stationary phase. Monocyclic pyrimidine nucleic acid bases (nucleobases) were reported to behave differently from their bicyclic purine analogs.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
120.2 °F - closed cup
flash_point_c
49 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 853(1-2), 114-122 (2007-04-03)
The influence of the chemical substitutions on the interfacial interactions of pyrimidines with the phospholipid-mimic immobilized-artificial-membrane (IAM) chromatographic stationary phase was evaluated. Monocyclic pyrimidine nucleic acid bases (nucleobases) were revealed behaving differently from their bicyclic purine counterparts substantially. The computed
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 63-63 (2015)
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