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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
120.2 °F - closed cup
Flash Point(C)
49 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 63-63 (2015)
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
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