23389-74-4

Basic information

• Product Name: 1-(4-Pyridinyl)hexane-1-one
• Synonyms: 1-(4-Pyridinyl)-1-hexanone;1-(4-Pyridinyl)hexane-1-one;1-Pyridin-4-yl-hexan-1-one
• CAS NO: 23389-74-4
• Molecular Formula: C11H15 N O
• Molecular Weight: 177.27
• Mol File: 23389-74-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 309.18°C (rough estimate)
• Flash Point: 131.1°C
• Appearance: /
• Density: 1.0290 (rough estimate)
• Vapor Pressure: 0.0037mmHg at 25°C
• Refractive Index: 1.5480 (estimate)
• Storage Temp.: 2-8°C
• PKA: 3.21±0.10(Predicted)
• CAS DataBase Reference: 1-(4-Pyridinyl)hexane-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Pyridinyl)hexane-1-one(23389-74-4)
• EPA Substance Registry System: 1-(4-Pyridinyl)hexane-1-one(23389-74-4)

Safety Data

• Hazardous Substances Data: 23389-74-4(Hazardous Substances Data)

Usage

Safety Profile

A poison by intraperitoneal route. A flammable liquid. When heated to decomposition it emits toxic vapors of NOx.

InChI:InChI=1/C11H15NO/c1-2-3-4-5-11(13)10-6-8-12-9-7-10/h6-9H,2-5H2,1H3

Upstream product

• 872-85-5 pyridine-4-carbaldehyde 
• 109-67-1 1-penten 
• 693-25-4 n-pentylmagnesium bromide 
• 23396-22-7 α-pentyl-4-pyridinemethanol 
• 1570-45-2 isonicotinic acid ethylester 
• 23708-48-7 pentamethylenebis(magnesium bromide) 

Relevant articles and documents

Comparative inhibition of tetrameric carbonyl reductase activity in pig heart cytosol by alkyl 4-pyridyl ketones

Context and objective: The present study is to elucidate the comparative inhibition of tetrameric carbonyl reductase (TCBR) activity by alkyl 4-pyridyl ketones, and to characterize its substrate-binding domain. Materials and methods: The inhibitory effect

Hydroacylation of 1-alkene with heteroaromatic aldehyde by Rh(I) and additives

Hydroacylation of 1-alkene with a heteroaromatic aldehyde such as pyridinecarboxaldehyde, thiophenecarboxaldehyde and furfural derivatives under cocatalyst of Wilkinson's complex and 2-amino-3-picoline gave poor yield of hydroacylated product. The addition of a catalytic amount of bis(cyclopentadienyl)zirconium dichloride or bis(cyclopentadienyl)titanium dichloride as an additive dramatically increased the yield of the hydroacylated ketone product.