132334-98-6

Basic information

• Product Name: ETHYL 6-BROMOPYRIDINE-3-CARBOXYLATE
• Synonyms: 6-BROMOPYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER;ETHYL 6-BROMOPYRIDINE-3-CARBOXYLATE;3-Pyridinecarboxylic acid, 6-broMo-, ethyl ester;6-BroMo-3-pyridinecarboxylic Acid Ethyl Ester;Ethyl 2-BroMo-5-pyridinecarboxylate;Ethyl 6-broMonicotinate
• CAS NO: 132334-98-6
• Molecular Formula: C8H8BrNO2
• Molecular Weight: 230.06
• Product Categories: Aromatics;Heterocycles;Nicotine Derivatives
• Mol File: 132334-98-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 292℃
• Flash Point: 131℃
• Appearance: /
• Density: 1.501
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: -1.14±0.10(Predicted)
• CAS DataBase Reference: ETHYL 6-BROMOPYRIDINE-3-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 6-BROMOPYRIDINE-3-CARBOXYLATE(132334-98-6)
• EPA Substance Registry System: ETHYL 6-BROMOPYRIDINE-3-CARBOXYLATE(132334-98-6)

Safety Data

• Hazardous Substances Data: 132334-98-6(Hazardous Substances Data)

Usage

Uses

A potential hypolipidemic agent; a nicotinic acid analog

Upstream product

• 6311-35-9 6-bromonicotinic acid 
• 64-17-5 ethanol 

Downstream Products

• 153559-73-0 ethyl 6-(1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)vinyl)nicotinate 
• 220882-43-9 ethyl 2-ethynylpyridine-5-carboxylate 

Relevant articles and documents

Synthesis of Functionalized Pyridines via a Regioselective Oxazoline Promoted C-H Amidation Reaction

The first Rh-catalyzed C-H amidation of pyridines is reported. The incorporation of a substituent at the C2 position both is crucial to the success of this transformation and provides considerable scope for further elaboration of the resulting products. Among these compounds, 2-chloropyridines allow access to a selection of intermediates including a versatile azaquinazoline scaffold.