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407070

Sigma-Aldrich

2-Chloro-4-(trifluoromethyl)pyrimidine

99%

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About This Item

Empirical Formula (Hill Notation):
C5H2ClF3N2
CAS Number:
Molecular Weight:
182.53
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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.)

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.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

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Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 63-63 (2015)
Hai-Bin Luo et al.
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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