97960-34-4

Basic information

• Product Name: Benzonitrile, 2-(2-propenyloxy)-
• CAS NO: 97960-34-4
• Molecular Formula: C10H9NO
• Molecular Weight: 159.188
• Mol File: 97960-34-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 2-(2-propenyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 2-(2-propenyloxy)-(97960-34-4)
• EPA Substance Registry System: Benzonitrile, 2-(2-propenyloxy)-(97960-34-4)

Safety Data

• Hazardous Substances Data: 97960-34-4(Hazardous Substances Data)

Upstream product

• 611-20-1 salicylonitrile 
• 106-95-6 allyl bromide 
• 14520-53-7 2-(prop-2'-enyloxy)benzamide 
• 53638-81-6 2,2’-(4-amino-4H-1,2,4-triazole-3,5-diyl)diphenol 
• 74255-21-3 2-hydroxybenzonitrile sodium salt 
• 6609-56-9 2-methoxy-benzonitrile 

Downstream Products

• 65-45-2 salicylamide 
• 93744-18-4 (S)-(+)-3-(2-cyanophenoxy)-1,2-epoxypropane 
• 46905-83-3 (S)-1-(2-cyanophenoxy)-2-hydroxy-3-tert-butylamino-propane 
• 850427-94-0 (R)-4-(2-cyanophenoxymethyl)-1,3,2-dioxathiolane-2,2-dioxide 
• 850427-88-2 (R)-4-(2-cyanophenoxymethyl)-1,3,2-dioxathiolane-2-oxide 
• 1054487-87-4 (2R)-1-(2-cyanophenoxy)-2,3-propanediol 
• 56715-37-8 (2S)-1-(2-cyanophenoxy)-2,3-propanediol 
• 515163-37-8 3-allyl-2-hydroxybenzonitrile 
• 161562-67-0 (2-prop-2-enoxyphenyl)methanamine 
• 14520-53-7 2-(prop-2'-enyloxy)benzamide 
• 611-20-1 salicylonitrile 
• 515163-42-5 7-cyano-2-methylbenzo[b]furan 

Relevant articles and documents

Palladium-Catalyzed Fluoroalkylative Cyclization of Olefins

A palladium-catalyzed fluoroalkylative cyclization of olefins with readily available Rf-I reagents to afford the corresponding fluoroalkylated 2,3-dihydrobenzofuran and indolin derivatives with moderate to excellent yields is reported. This novel procedure provides an efficient method for the construction of Csp3-CF2 and C-O/N bonds in one step. A wide range of functional groups are tolerated. It is proposed that a radical/SET (single electron transfer) pathway proceeding via the fluoroalkyl radical may be involved in the catalytic cycle.

Surfactant-mediated solvent-free dealkylative cleavage of ethers and esters and trans-alkylation under neutral conditions

A simple, surfactant-mediated, one-pot, solvent-free dealkylative cleavage of aryl ethers and esters followed by subsequent optional trans-alkylation under essentially neutral conditions has been developed.

A facile synthesis of benzofuran derivatives: A useful synthon for preparation of trypsin inhibitor

Mono-substituted 2-methylbenzo[b]furans were prepared by Claisen rearrangement of corresponding allyl phenyl ethers and subsequent bis(benzonitrile)palladium(II) chloride-mediated cyclization of o-allylphenols.