Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

407070

Sigma-Aldrich

2-Chloro-4-(trifluoromethyl)pyrimidine

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C5H2ClF3N2
CAS Number:
33034-67-2
Molecular Weight:
182.53
MDL number:
MFCD00115111
UNSPSC Code:
12352100
PubChem Substance ID:
24865422
NACRES:
NA.22

Quality Level

100

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
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 63-63 (2015)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service