17755-30-5

Basic information

• Product Name: Pyridine, 4-(1-methylethenyl)-
• CAS NO: 17755-30-5
• Molecular Formula: C8H9N
• Molecular Weight: 119.166
• Mol File: 17755-30-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Pyridine, 4-(1-methylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 4-(1-methylethenyl)-(17755-30-5)
• EPA Substance Registry System: Pyridine, 4-(1-methylethenyl)-(17755-30-5)

Safety Data

• Hazardous Substances Data: 17755-30-5(Hazardous Substances Data)

Upstream product

• 40473-14-1 2-chloro-2-(4-pyridyl)propane 
• 930-69-8 sodium thiophenolate 
• 3958-63-2 lithium 2-nitropropane 
• 25128-23-8 2,3-dimethyl-2,3-di-4-pyridylbutane 
• 696-30-0 4-s-propylpyridine 
• 536-75-4 4-Ethylpyridine 

Downstream Products

• 696-30-0 4-s-propylpyridine 
• 1122-54-9 methyl (4-pyridyl) ketone 
• 75-89-8 2,2,2-trifluoroethanol 
• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 79190-35-5 1-mercaptophenyl-2-(4-pyridyl)propane 

Relevant articles and documents

Alkylpyridines transformations over acidic catalysts. An example of radical reactions on ionic surfaces

4-Methyl-, 4-ethyl-, and 4-isopropylpyridine, ethyl-, and isopropylbenzene transformations were studied over the series of amorphous silica-aluminas. The main reactions of alkylpyridines were the transformations of the alkyl side chain. The crucial role of one-electron donor (radical) centres in the mentioned reactions was evidenced by the physicochemical characterization of the catalyst surfaces, the apparent correlation of activity vs. active centres concentration, and the dependence of product composition upon reaction conditions.

Reactions of 2-Chloro-2-(4-pyridyl)propane with Nucleophiles. Substitution on Tertiary Carbon

The reaction of 2-chloro-2-(4-pyridyl)propane (2) with lithium 2-propanenitronate affords the C-alkylation product 2-nitro-3-(4-pyridyl)-2,3-dimethylbutane (3), the Michael-adduct 2-nitro-2-methyl-4-(4-pyridyl)pentane (4), 4-isopropenylpyridine (5) and 2-