74317-85-4

Basic information

• Product Name: 3-(2-AMINOETHYL)PYRIDINE
• Synonyms: p-Anisicacid, 2-bromo- (6CI);2-Bromo-p-anisic acid, 3-Bromo-4-carboxyanisole;Benzoicacid, 2-broMo-4-Methoxy-
• CAS NO: 74317-85-4
• Molecular Formula: C₈H₇BrO₃
• Molecular Weight: 231.05
• EINECS: 214-589-6
• Product Categories: Pyridine
• Mol File: 74317-85-4.mol
• Article Data: 14

Chemical Properties

• Melting Point: 199℃
• Boiling Point: 313.6 °C at 760 mmHg
• Flash Point: 143.5 °C
• Appearance: /
• Density: 1.625±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.000209mmHg at 25°C
• Refractive Index: 1.583
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.12±0.10(Predicted)
• CAS DataBase Reference: 3-(2-AMINOETHYL)PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-AMINOETHYL)PYRIDINE(74317-85-4)
• EPA Substance Registry System: 3-(2-AMINOETHYL)PYRIDINE(74317-85-4)

Safety Data

• Hazardous Substances Data: 74317-85-4(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1/C8H7BrO3/c1-12-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)

Upstream product

• 36942-56-0 3-bromo-4-methylanisole 
• 59142-57-3 (2-bromo-4-methoxyphenyl)phenylmethanone 
• 17100-65-1 2-bromo-4-methoxybenzoic acid methyl ester 
• 4294-95-5 4-methoxyanthranilic acid 
• 100-09-4 4-methoxybenzoic acid 
• 1208075-63-1 2-bromo-4-methoxybenzoic acid ethyl ester 
• 60710-39-6 3-bromo-p-cresol 
• 28547-28-6 2-bromo-4-hydroxybenzoic acid 
• 77-78-1 dimethyl sulfate 
• 140860-51-1 2-bromo-4-methoxy benzonitrile 
• 43192-31-0 2-bromo-4-methoxybenzaldehyde 
• 2398-37-0 3-methoxyphenyl bromide 
• 89691-67-8 1-(2-bromo-4-methoxyphenyl)ethanone 

Downstream Products

• 28547-28-6 2-bromo-4-hydroxybenzoic acid 
• 1293285-11-6 4-methoxy-2-(2H-1,2,3-triazol-2-yl)benzoic acid 
• 1307741-22-5 N-butyl-2-bromo-N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-4-methoxybenzamide 
• 246231-75-4 7-methoxy-2-phenylquinazolin-4(3H)-one 
• 1432371-67-9 2-bromo-N-cyclopropyl-4-methoxy-N-methylbenzamide 
• 1446086-67-4 benzyl 2-bromo-4-hydroxybenzoate 
• 1446086-68-5 benzyl 2-(3-carbamoylphenyl)-4-hydroxybenzoate 
• 1446086-69-6 cyclohexylcarbamic acid 6-benzyloxycarbonyl-3′-carbamoylbiphenyl-3-yl ester 
• 1425459-40-0 cyclohexylcarbamic acid 3′-carbamoyl-6-carboxybiphenyl-3-yl ester 

Relevant articles and documents

Photoinduced Carbon Tetrabromide Initiated Aerobic Oxidation of Substituted Toluenes to Carboxylic Acids

A mild and metal-free procedure is reported for the aerobic oxidation of substituted toluenes to carboxylic acids by using CBr 4 as initiator under irradiation from a 400 nm blue light-emitting diode.

METHOD FOR PRODUCING 2-HALOGENATED BENZOIC ACIDS

The purpose of the present invention is to provide a method for producing 2-halogenated benzoic acids, the method imparting high regioselectivity (high selectivity) and having a shorter reaction time than does the conventional reaction. This method for producing 2-halogenated benzoic acids, in order to achieve the above purpose, is characterized in that benzoic acids and a halogenating agent are reacted in the presence of an alkaline compound, making it possible to highly selectively obtain 2-halogenated benzoic acids.

ENHANCING AUTOPHAGY OR INCREASING LONGEVITY BY ADMINISTRATION OF UROLITHINS OR PRECURSORS THEREOF

Disclosed are methods, compounds, and compositions useful for increasing autophagy and promoting longevity. The methods, compounds, and compositions relate to urolithins and urolithin precursors and use thereof. Certain urolithins are represented by Formula I, while certain urolithin precursors are represented by Formula IV. The urolithin may be urolithin A, urolithin B, urolithin C, or urolithin D. The urolithin precursor may be ellagic acid or an ellagitannin. The methods include in vivo, ex vivo, and in vitro uses of the compounds and compositions.