850429-51-5

Basic information

• Product Name: ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE
• Synonyms: ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE;ETHYL 6-AMINO-5-BROMONICOTINATE;Ethyl 6-amino-5-bromonicotinate 98%;Ethyl 2-amino-3-bromopyridine-5-carboxylate;3-Pyridinecarboxylic acid, 6-aMino-5-broMo-, ethyl ester;6-AMino-5-broMo-nicotinic acid ethyl ester;6-Amino-5-bromo-3-pyridinecarboxylic acid ethyl ester;Ethyl6-amino-5-bromonicotinate98%
• CAS NO: 850429-51-5
• Molecular Formula: C₈H₉BrN₂O₂
• Molecular Weight: 245.07
• Product Categories: Amines;blocks;Bromides;Carboxes;Pyridines
• Mol File: 850429-51-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 125-127
• Boiling Point: 335.1 °C at 760 mmHg
• Flash Point: 156.4 °C
• Appearance: /
• Density: 1.575 g/cm³
• Vapor Pressure: 0.000123mmHg at 25°C
• Storage Temp.: Keep Cold
• PKA: 2.12±0.49(Predicted)
• CAS DataBase Reference: ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE(850429-51-5)
• EPA Substance Registry System: ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE(850429-51-5)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 850429-51-5(Hazardous Substances Data)

Usage

General Description

ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE is a chemical compound with the molecular formula C8H8BrN2O2. It is a derivative of pyridine and contains an amino group, a bromine atom, and a carboxylate group. ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, including its antimicrobial and anti-inflammatory properties. Due to its versatile nature and potential applications, ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE is a valuable compound in various fields of research and industry.

InChI:InChI=1/C8H9BrN2O2/c1-2-13-8(12)5-3-6(9)7(10)11-4-5/h3-4H,2H2,1H3,(H2,10,11)/p+1

Upstream product

• 3167-49-5 6-aminonicotinic acid 
• 39658-41-8 ethyl-6-amino-nicotinate 

Downstream Products

• 1027785-04-1 ethyl 6-amino-5-(phenylethynyl)nicotinate 
• 1027785-19-8 (6-amino-5-bromopyridin-3-yl)methanol 
• 957103-97-8 8-bromoimidazo[1,2-a]pyridine-6-carboxylic acid ethyl ester 
• 180340-69-6 6-Amino-5-bromopyridine-3-carboxylic acid 
• 1027785-06-3 2-phenyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid 
• 1616385-54-6 N-(4,5-dimethyl-1H-pyrazol-3-yl)-2-phenyl-1H-pyrrolo[2,3-b]pyridine-5-carboxamide 

Relevant articles and documents

ISOPROPYL TRIAZOLO PYRIDINE COMPOUNDS

The present invention provides a compound of the Formula (I) below: Wherein R1 is selected from the group consisting of H, CH3, CN, CH2CN, C(CH3)2CN, and F; R2 is selected from the group consisting of H, O(C1-C3alkyl)R5, CH2CN, and CN; R3 is selected from the group consisting of H, OCH3, CN, C(CH3)2CN, and CH2CN; R4 is selected from the group consisting of H and CH3; R5 is selected from the group consisting of H, CN, C(CH3)2CN, OCH3, S(O)2CH3, and C(CH3)2OH; provided that at least one selected from the group consisting of R1, R2, R3 and R4 is H; or a pharmaceutically acceptable salt thereof, methods of treating diabetes using the compound and a process for preparing the compound.

P2X3 AND/OR P2X2/3 COMPOUNDS AND METHODS

The present application provides novel compounds and methods for preparing and using these compounds. In one embodiment, the compounds are of the structure of formula (I), wherein R1-R4 are defined herein. In a further embodiment, these compounds are useful in method for regulating one or both of the P2X3 or P2X2/3 receptors. In another embodiment, these compounds are useful for treating pain in patients by administering one or more of the compounds to a patient.