4357-31-7

Basic information

• Product Name: 4-(4-Ethoxyphenyl)pyridine
• Synonyms: 4-(4-Ethoxyphenyl)pyridine
• CAS NO: 4357-31-7
• Molecular Formula: C₁₃H₁₃NO
• Molecular Weight: 199.24842
• Mol File: 4357-31-7.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(4-Ethoxyphenyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-Ethoxyphenyl)pyridine(4357-31-7)
• EPA Substance Registry System: 4-(4-Ethoxyphenyl)pyridine(4357-31-7)

Safety Data

• Hazardous Substances Data: 4357-31-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-(4-Ethoxyphenyl)pyridine is used as a pharmaceutical intermediate for the synthesis of active pharmaceutical ingredients. It plays a crucial role in the development of new drugs and contributes to the advancement of medicine.
Used in Agrochemical Industry:
4-(4-Ethoxyphenyl)pyridine is used as an intermediate in the synthesis of agrochemicals. It helps in the development of effective pesticides and other agricultural chemicals, ensuring better crop protection and yield.
Used in Material Science:
4-(4-Ethoxyphenyl)pyridine has potential applications in material science. Its unique properties and structure make it a valuable component in the creation of new materials with specific characteristics for various industries.

Upstream product

• 110-86-1 pyridine 
• 38793-99-6 4-ethoxy-benzenediazonium; chloride 
• 3108-14-3 4-ethoxyphenylphenyldiazonium tetrafluoroborate 
• 699-08-1 1-ethoxy-4-iodobenzene 
• 1692-15-5 4-pyridylboronic acid 
• 1120-87-2 4-bromopyridin 
• 90591-48-3 tris-(4-ethoxy-phenyl)-bismuthine 

Downstream Products

• 760150-51-4 4-(4-ethoxy-phenyl)-piperidine 
• 1444778-48-6 (S)-1-cyano-cyclopropanecarboxylic acid (1-{4-[4-(4-ethoxy-phenyl)-piperidin-1-yl]-phenyl}-ethyl)-amide 
• 1444779-19-4 (S)-N-(1-{4-[4-(4-ethoxy-phenyl)-piperidin-1-yl]-phenyl}-ethyl)-N-methyl-acetamide 
• 1444778-76-0 (S)-2-acetylamino-oxazole-4-carboxylic acid (1-{4-[4-(4-ethoxy-phenyl)-piperidin-1-yl]-phenyl}-ethyl)-amide 
• 1444779-16-1 (S)-(1-{4-[4-(4-ethoxy-phenyl)-piperidin-1-yl]-phenyl}-ethyl)-carbamic acid methyl ester 
• 1444779-04-7 (S)-3-(1-{4-[4-(4-ethoxy-phenyl)-piperidin-1-yl]-phenyl}-ethyl)-1-ethyl-1-methyl-urea 
• 1444780-57-7 (S)-1-{4-[4-(4-ethoxy-phenyl)-piperidin-1-yl]-phenyl}-ethylamine hydrochloride 

Relevant articles and documents

Triarylbismuthanes as threefold aryl-transfer reagents in regioselective cross-coupling reactions with bromopyridines and quinolines

Cross-coupling studies using bromopyridines and bromoquinolines with triarylbismuths as threefold coupling reagents in substoichiometric amounts under Pd-catalysed conditions are disclosed. The reactivity was high with both mono- and dibromopyridyl substrates, and mono- and bis-couplings were carried out regioselectively. A library of monoaryl and diaryl pyridines was formed in high yields. A one-pot strategy provided a simple and straightforward synthesis of both symmetrical and unsymmetrical diarylpyridines. Arylations of 2-bromo- and 3-bromoquinolines were achieved with triarylbismuth reagents. This study demonstrates that triarylbismuths may be used as threefold arylating reagents for the synthesis of aryl pyridines and quinolines through couplings with bromopyridines and bromoquinolines under Pd-catalysed conditions. Copyright

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