1171919-08-6

Basic information

• Product Name: Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate
• Synonyms: Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate;Ethyl 4-(trifluoromethyl)pyridine-2-carboxylate;Ethyl 4-(trifluoromethyl)picolinate
• CAS NO: 1171919-08-6
• Molecular Formula: C9H8F3NO2
• Molecular Weight: 219.1605296
• Mol File: 1171919-08-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate(1171919-08-6)
• EPA Substance Registry System: Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate(1171919-08-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1171919-08-6(Hazardous Substances Data)

Usage

General Description

Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate is a specialized chemical compound that falls under the category of organofluorines, which are organic compounds that contain a fluorine atom. Its molecular formula is C10H10F3NO2. Ethyl 4-(trifluoromethyl)-2-pyridinecarboxylate has certain industrial and research oriented applications due to its unique reactive properties. It is often used as an intermediate substance in organic chemistry, serving as a building block in synthesizing and manufacturing more complex chemicals or compounds. It's important to handle this chemical carefully as it may pose certain hazard risks, therefore usage should follow specific safety measures and precautions.

Upstream product

• 109-94-4 formic acid ethyl ester 
• 175205-81-9 2-bromo-4-(trifluoromethyl)pyridine 

Downstream Products

• 939047-74-2 ethyl 6-chloro-4-(trifluoromethyl)picolinate 

Relevant articles and documents

Engineering High-Potential Photo-oxidants with Panchromatic Absorption

Challenging photochemistry demands high-potential visible-light-absorbing photo-oxidants. We report (i) a highly electron-deficient Ru(II) complex (eDef-Rutpy) bearing an E1/20/+ potential more than 300 mV more positive than that of any established Ru(II) bis(terpyridyl) derivative, and (ii) an ethyne-bridged eDef-Rutpy-(porphinato)Zn(II) (eDef-RuPZn) supermolecule that affords both panchromatic UV-vis spectral domain absorptivity and a high E1/20/+ potential, comparable to that of Ce(NH4)2(NO3)6 [E1/2(Ce3+/4+) = 1.61 V vs NHE], a strong and versatile ground-state oxidant commonly used in organic functional group transformations. eDef-RuPZn exhibits ～8-fold greater absorptive oscillator strength over the 380-700 nm range relative to conventional Ru(II) polypyridyl complexes, and impressive excited-state reduction potentials (1E-/? = 1.59 V; 3E-/? = 1.26 V). eDef-RuPZn manifests electronically excited singlet and triplet charge-transfer state lifetimes more than 2 orders of magnitude longer than those typical of conventional Ru(II) bis(terpyridyl) chromophores, suggesting new opportunities in light-driven oxidation reactions for energy conversion and photocatalysis.

Synthesis method of 2-pyridylaldehyde derivative

The invention relates to the field of medical intermediates, in particular to a synthesis method of 2-pyridylaldehyde derivative. A synthesis path shown in the formula 1 is adopted, wherein X can be Cl or Br or CF3. Cheap starting raw materials are adopted, the use of hazardous materials which have large toxicity and are easily explosive is avoided, the cost of the product is greatly lowered, popularization and industrialized production are facilitated, and the synthesis method has the advantages of being low in cost, easy to operate, high in yield, easy to industrialize and the like. The formula 1 is shown in the description.