898776-54-0

Basic information

• Product Name: ETHYL 5-OXO-5-(2-PYRIDYL)VALERATE
• Synonyms: ETHYL 5-OXO-5-(2-PYRIDYL)VALERATE
• CAS NO: 898776-54-0
• Molecular Formula: C12H15NO3
• Molecular Weight: 221.25
• Mol File: 898776-54-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 345.7°C at 760 mmHg
• Flash Point: 162.9°C
• Appearance: /
• Density: 1.105g/cm³
• Vapor Pressure: 6.04E-05mmHg at 25°C
• Refractive Index: 1.504
• CAS DataBase Reference: ETHYL 5-OXO-5-(2-PYRIDYL)VALERATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 5-OXO-5-(2-PYRIDYL)VALERATE(898776-54-0)
• EPA Substance Registry System: ETHYL 5-OXO-5-(2-PYRIDYL)VALERATE(898776-54-0)

Safety Data

• Hazardous Substances Data: 898776-54-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H15NO3/c1-2-16-12(15)8-5-7-11(14)10-6-3-4-9-13-10/h3-4,6,9H,2,5,7-8H2,1H3

Upstream product

• 108-55-4 glutaric anhydride, 
• 64-17-5 ethanol 
• 157730-57-9 5-hydroxy-1(pyridin-2-yl)pentan-1-one 
• 109-04-6 2-bromo-pyridine 
• 10198-89-7 1-(2-pyridyl)-3-(2-pyridyl)-1,3-propanedione 
• 140-88-5 ethyl acrylate 
• 13672-84-9 5-(2-pyridyl)-5-oxopentanoic acid 

Relevant articles and documents

Inorganic alkali catalytic 1, 5 - ketonic ester apperception compound synthesis method

The invention discloses a synthesis method for a 1,5-ketonic ester compound under catalyzing of inorganic base. The synthesis method comprises the following steps: taking a compound of the general formula I as a raw material, taking inorganic base as a ca

Catalytic asymmetric hydrogenation of δ-ketoesters: Highly efficient approach to chiral 1,5-diols

High turnover: An highly efficient catalytic asymmetric hydrogenation of δ-aryl-δ-ketoesters has been realized by using the chiral spiroiridium catalyst (R)-1. Chiral 1,5-diol products are obtained with excellent enantioselectivity and turnover numbers (TONs) as high as 100 000. TOF=turnover frequency. Copyright