6749-54-8

Upstream product

• 98-85-1 1-Phenylethanol 
• 13466-30-3 1-(2-methylphenyl)hydrazonoethane 
• 75067-08-2 benzene 

Downstream Products

• 4013-34-7 3-phenyl-2-oxabutane 
• 33863-82-0 4-methyl-N-(1-phenylethyl)aniline 
• 881846-79-3 4-chloro-N-(1-phenylethyl)benzenamine 
• 5350-86-7 anti-2,3-Diphenylbutanoic acid 
• 5350-86-7 syn-2,3-Diphenylbutanoic acid 
• 1092840-22-6 N'-phenylhydrazine carboxylic acid 1-phenylethyl ester 
• 2040-37-1 benzyl 1-phenylethyl ether 
• 259195-14-7 trithiocarbonic acid bis(1-phenylethyl) ester 
• 1138320-58-7 N'-phenylhydrazinecarbodithioic acid 1-phenylethyl ester 
• 126522-56-3 4-methoxy-N-(1-phenylethyl)aniline 
• 14034-63-0 3-nitroanilinium 4-toluenesulfonate 
• 135787-34-7 3-nitro-N-[1-(phenyl)ethyl]aniline 

Relevant academic research and scientific papers

Reaction of Hydrazones with Methoxy(tosyloxy)iodobenzene (MTIB): Tosylate Formation under Oxidative Conditions

Treatment of aromatic hydrazones 1 containing electron-withdrawing, reduction sensitive substituents with MTIB gives the corresponding tosylates 2 in high yield. When the tosylate is particularly reactive the thermodynamically more stable methyl ether 3 is isolated. Analogous reactions with DAIB give acetates 4 in high yield. Dialkyl hydrazones give olefinic products (e.g. 7 and 8). (+)-Camphor hydrazone 1k with either MTIB or DAIB gives both camphene 12 (major product) and tricyclene 11 (minor product) suggesting that a carbene pathway accounts for some of the material formed in these oxidations.

Nucleophilic Substitiution Reactions of 1-Phenylethyl Benzenesulfonates with Anilines in Methanol-Acetonitrile

Nucleophilic substitution reactions of 1-phenylethyl benzenesulfonates with anilines have been investigated in methanol-acetonitrile mixtures at 25 deg C.Magnitudes of the Hammett coefficients ρX, ρY, and ρZ indicate that

Arylalkyl amines useful for lowering intraocular pressure

Intraocular hypertensive diseases such as glaucoma are treated with compounds represented by formula I STR1 or a pharmaceutically acceptable acid addition salt thereof, wherein R1 is alkyl of two to four carbon atoms; R2 is --(CH2)n --C6 H4 --R5 ; where n is an integer from 1 to 4; and R5 is --H, --OH, halo, lower alkyl, lower alkoxy, ureido, lower alkyl-ureido, lower alkyl-amido, or formamido; R3 is hydro or hydroxy; and R4 is hydro, lower alkyl, amino, or lower alkylamino.