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2-Chloro-4-(trifluoromethyl)pyridine
[CAS# 81565-18-6]

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Complete supplier list of 2-Chloro-4-(trifluoromethyl)pyridine
Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyridine compound >> Methylpyridine
Name 2-Chloro-4-(trifluoromethyl)pyridine
Molecular Structure CAS # 81565-18-6, 2-Chloro-4-(trifluoromethyl)pyridine
Molecular Formula C6H3ClF3N
Molecular Weight 181.54
CAS Registry Number 81565-18-6
EC Number 617-242-3
SMILES C1=CN=C(C=C1C(F)(F)F)Cl
Properties
Density 1.411
Melting point -19 ºC
Boiling point 146-147 ºC
Refractive index 1.4490
Flash point 40 ºC
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS07 Warning    Details
Hazard Statements H226-H302-H312-H315-H319-H335    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P370+P378-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Flammable liquidsFlam. Liq.3H226
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H312
Eye irritationEye Irrit.2AH319
Acute toxicityAcute Tox.3H331
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.4H332
Transport Information UN 1993
SDS Available
up Discovory and Applicatios
2-Chloro-4-(trifluoromethyl)pyridine is a significant chemical compound known for its versatility in various industrial and scientific applications. The discovery and subsequent utilization of this compound have made considerable impacts in the fields of pharmaceuticals, agrochemicals, and materials science.

2-Chloro-4-(trifluoromethyl)pyridine is a halogenated pyridine derivative. Its structure consists of a pyridine ring with a chlorine atom at the second position and a trifluoromethyl group at the fourth position. This particular arrangement of functional groups imparts unique chemical properties to the compound, making it highly valuable as an intermediate in organic synthesis.

The discovery of 2-Chloro-4-(trifluoromethyl)pyridine can be traced back to the mid-20th century when chemists were exploring new ways to introduce trifluoromethyl groups into aromatic compounds. The trifluoromethyl group is well-known for its ability to enhance the biological activity, stability, and lipophilicity of organic molecules. This made 2-Chloro-4-(trifluoromethyl)pyridine an attractive target for synthesis and study.

In the pharmaceutical industry, 2-Chloro-4-(trifluoromethyl)pyridine is widely used as a building block for the synthesis of various bioactive compounds. Its structure allows for the introduction of other functional groups, facilitating the creation of complex molecules with potential therapeutic effects. Researchers have utilized this compound in the development of drugs targeting a range of conditions, from infectious diseases to cancer. The presence of the trifluoromethyl group often enhances the efficacy and pharmacokinetic properties of these drugs.

In agrochemicals, 2-Chloro-4-(trifluoromethyl)pyridine plays a crucial role in the synthesis of herbicides, fungicides, and insecticides. Its ability to act as a precursor in the creation of active ingredients helps in producing compounds that are more effective and selective against pests and diseases. The compound’s chemical stability and ability to enhance the bioactivity of agrochemicals contribute to improved crop protection and yield.

Moreover, 2-Chloro-4-(trifluoromethyl)pyridine is also utilized in materials science. Its incorporation into polymers and other materials can impart desirable properties such as increased thermal stability, chemical resistance, and hydrophobicity. These characteristics are valuable in the development of advanced materials for various industrial applications, including coatings, electronics, and specialty chemicals.

The synthesis of 2-Chloro-4-(trifluoromethyl)pyridine typically involves halogenation and trifluoromethylation reactions. Advances in synthetic methodologies have improved the efficiency and yield of these processes, making the compound more accessible for research and industrial use.
Market Analysis Reports
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