185847-84-1

Basic information

• Product Name: Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate
• Synonyms: Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate;Benzyl 4-oxo-1,2,3,4-tetrahydropyridine-1-carboxylate;Benzyl3,4-dihydro-4-oxo-pyridine-1(2H)-carboxylate;Benzyl 4-oxo-3,4-dihydropyridine-1(2H)
• CAS NO: 185847-84-1
• Molecular Formula: C₁₃H₁₃NO₃
• Molecular Weight: 231.25
• Mol File: 185847-84-1.mol
• Article Data: 17

Chemical Properties

• Melting Point: 72-73 °C
• Boiling Point: 382.2°C at 760 mmHg
• Flash Point: 184.9°C
• Appearance: /
• Density: 1.245g/cm³
• Vapor Pressure: 4.81E-06mmHg at 25°C
• Refractive Index: 1.58
• Storage Temp.: 2-8°C
• PKA: -4.31±0.20(Predicted)
• CAS DataBase Reference: Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate(185847-84-1)
• EPA Substance Registry System: Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate(185847-84-1)

Safety Data

• Hazardous Substances Data: 185847-84-1(Hazardous Substances Data)

Usage

General Description

Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate is a chemical compound with the molecular formula C16H15NO3. It is a dihydropyridine derivative with a benzyl group and a carboxylic ester group. Benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate has potential pharmaceutical applications, particularly in the field of cardiovascular medicine. Dihydropyridine derivatives are known to have calcium channel blocking properties, which can help in the treatment of hypertension and angina. The benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate compound may also have other biological activities and may be used as a building block in the synthesis of other organic compounds. Its specific properties and potential uses would require further research and testing.

InChI:InChI=1/C13H13NO3/c15-12-6-8-14(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-6,8H,7,9-10H2

Upstream product

• 66207-23-6 1-benzyloxycarbonyl-1,2,3,6-tetrahydropyridine 
• 68471-58-9 1-(benzyloxycarbonyl)-1,2,3,4-tetrahydropyridine 
• 501-53-1 benzyl chloroformate 
• 40064-34-4 piperidine-4,4-diol hydrochloride 
• 19099-93-5 benzyl 4-oxo-1-piperidinecarboxylate 
• 940925-56-4 benzyl 6-bromo-1,4-dioxa-8-azaspiro[4.5]decane-8-carboxylate 
• 620-08-6 4-methoxypyridine 
• 53708-19-3 4-isopropoxypyridine 

Downstream Products

• 68471-58-9 1-(benzyloxycarbonyl)-1,2,3,4-tetrahydropyridine 
• 717920-53-1 (R)-2-(4-fluoro-2-methylphenyl)-4-piperidinone-1-carboxylate 
• 335266-05-2 (R)-4-oxo-2-phenyl-piperidine-1-carboxylic acid benzyl ester 
• 414910-20-6 (R)-2-(4-Fluoro-phenyl)-4-oxo-piperidine-1-carboxylic acid benzyl ester 
• 852051-10-6 (R)-1-benzyloxycarbonyl-2-methyl-4-piperidone 

Relevant articles and documents

Synthesis of Novel Iminosugar Derivatives Based on a 2-Azabi-ccyclo[41.0]heptane Skeleton

Iminosugars are good starting points for the development of different kinds of drugs. Many are polyhydroxylated piperidines that behave as biomimetics of their corresponding pyranoses analogues. In the interaction with carbohydrate processing enzymes, sel

An efficient synthesis of cis-4-hydroxyphosphonic and cis-4-hydroxyphosphinic analogs of pipecolic acid from cyclic enaminones

An expedient synthetic entry to cis-4-hydroxyphosphonic and cis-4-hydroxyphosphinic analogs of cis-4-hydroxypipecolic acid is presented in this paper. The main feature of this methodology is the highly regioselective addition of silyl phosphites or phosph

CHEMICAL PROCESS FOR PREPARING PHENYLPIPERIDINYL INDOLE DERIVATIVES

The present invention relates to a method of synthesizing a compound of formula (I) also referred to as 4-((2S,4S)-(4-ethoxy-1-((5-methoxy-7-methyl-1H-indol-4-yl)methyl)piperidin-2-yl))benzoic acid, or a pharmaceutically acceptable salt thereof, and/or intermediates thereof, their use as pharmaceuticals and pharmaceutical compositions and the use of intermediates for preparing a compound of formula (I), or a pharmaceutically acceptable salt thereof.