34577-38-3

Basic information

• Product Name: 2-Methyl-1-(α-naphthyl)-2-propanol
• Synonyms: 2-Methyl-1-(α-naphthyl)-2-propanol
• CAS NO: 34577-38-3
• Molecular Weight: 200.28
• Mol File: 34577-38-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Methyl-1-(α-naphthyl)-2-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-1-(α-naphthyl)-2-propanol(34577-38-3)
• EPA Substance Registry System: 2-Methyl-1-(α-naphthyl)-2-propanol(34577-38-3)

Safety Data

• Hazardous Substances Data: 34577-38-3(Hazardous Substances Data)

Upstream product

• 2876-78-0 methyl 1-naphthylacetate 
• 75-16-1 methylmagnesium bromide 
• 86-87-3 naphth-1-yl acetic acid 
• 6245-96-1 α-naphthylmethyl phenyl ether 
• 67-63-0 isopropyl alcohol 
• 917-64-6 methyl magnesium iodide 

Downstream Products

• 217480-50-7 4-chloromethyl-2,2-dimethyl-1,2-dihydrobenzo[f]isoquinoline 
• 1427307-52-5 2,2-dimethyl-4-(2-furyl)-1,2-dihydrobenzo[f]iso-quinoline 

Relevant articles and documents

(ALPHA-SUBSTITUTED ARALKYLAMINO AND HETEROARYLALKYLAMINO) PYRIMIDINYL AND 1,3,5-TRIAZINYL BENZIMIDAZOLES, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR USE IN TREATING PROLIFERATIVE DISEASES

Provided herein are (alpha-substituted aralkylamino or heteroarylalkylamino) pyrimidinyl and 1,3,5-triazinyl benzimidazoles, e.g., a compound of Formula 1, and their pharmaceutical compositions, preparation, and use as agents or drugs for treating proliferative diseases

CLEVEAGE RATES FOR RADIOLYSIS-PRODUCED RADICAL ANIONS OF NAPHTHYLMETHYL PHENYL ETHERS AND NAPHTHYL BENZYL ETHERS

Cleveage reactions of α- and β-naphthylmethyl phenyl ethers and of α- and β-naphthyl benzyl ethers were studied by pulse radiolysis.Transient spectra indicate that reactions occur via electron capture followed by cleavage of the resultant radical anions to give arylmethyl radicals and aryloxide ions.Product studies of extensively irradiated samples are consistent with this scheme and show patterns which are informative for radiation studies in general.The reactions were studied in several solvents.The behavior of transient spectra obtained in acetonitrile for these ethers shows clearly that radical anions of the naphthylmethyl ethers cleave more rapidly than do the radical anions of the naphthyl benzyl ethers.