62170-45-0

Usage

Chemical Structure

It has a butene backbone.
A cyanophenyl group is attached to the fourth carbon of the butene backbone.

Nature

Unsaturated organic compound

Applications

Used in the synthesis of pharmaceuticals, agrochemicals, and organic compounds.
Acts as a building block in the production of other chemicals and materials.
Utilized in academic research and chemical reactions to study its properties and behavior.

InChI:InChI=1/C11H11N/c1-2-3-6-10-7-4-5-8-11(10)9-12/h2,4-5,7-8H,1,3,6H2

Upstream product

• 529-19-1 2-Methylbenzonitrile 
• 106-95-6 allyl bromide 
• 13203-73-1 2-methylene-1-tetralone 
• 119220-52-9 2-Trimethylsilanylmethyl-3,4-dihydro-2H-naphthalen-1-one 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 612-13-5 2-cyanobenzyl chloride 
• 5162-44-7 1-bromo-4-butene 
• 91-15-6 phthalonitrile 
• 119204-69-2 2-Trimethylsilanylmethyl-3,4-dihydro-2H-naphthalen-1-one oxime 
• 7051-34-5 cyclopropylcarbinyl bromide 
• 119204-71-6 C₁₆H₂₃NO₂Si 
• 119204-70-5 C₁₆H₂₃NO₂Si 

Downstream Products

• 1122061-72-6 (2-(but-3-en-1-yl)phenyl)methanamine 

Relevant academic research and scientific papers

Efficient preparation method of 1-aryl-4-butene compound

The invention belongs to the technical field of fine chemicals and related chemistry, and provides an efficient preparation method of a 1-aryl-4-butene compound. The 1-aryl-4-butene compound can be obtained by taking halogen-containing methyl aromatic hyd

Synthesis of phthalonitriles containing ω-alkenyl, ω-(alkylsulfanyl)alkyl, and ω-(alkylsulfonyl)alkyl substituents and phthalocyanine derivatives based thereon

Alkylation of phthalonitrile radical anion sodium salt with terminal alkenyl bromides (4-bromobut-1-ene, 5-bromopent-1-ene, and 6-bromohex-1-ene) gave the corresponding 4-alkenylphthalonitriles which reacted with alkanethiols (BuSH and n-C10Hs

Coupling of β-cyanocarbene-chromium complexes with 2-alkynylbenzoyl derivatives: A [5+5]-cycloaddition approach to phenanthridines

The coupling of β-cyanocarbene complexes and 2-alkynylbenzoyl derivatives has been examined. The reaction afforded phenanthridine derivatives in a complex tandem process involving carbene-alkyne coupling, isobenzofuran formation, intramolecular Diels-Alder reaction using a nitrile dienophile, and deoxygenation. The chemistry could not be reproduced in non-chromium-based systems. Georg Thieme Verlag Stuttgart.

Reductive activation of arenes: XIX. Mechanism and some synthetic applications of the alkylation of phthalodinitrile radical anion

Using cyclopropylmethyl bromide as mechanism-sensitive reagent, it was shown that the reaction of phthalonitrile radical anion with alkyl halides in liquid ammonia involves electron transfer. The effects of the nature of alkyl bromide and counterion in th

SILICON-DIRECTED BECKMANN FRAGMENTATION

The selective fragmentation reactions of β-trimethylsilylketoximes have been proved to proceed effectively with acid catalysts giving the corresponding nitriles.Cyclic silylketoximes gave unsaturated nitriles.The fragmentation in the Beckmann rearrangement is completely controlled and directed by a trimethylsilyl group to lead the regio- and stereo-specific formation of the double bond.The catalytic fragmentation proceeds with the combination of trimethylsilyl ketoxime acetates and trimethylsilyl trifluoromethanesulfonate giving nitriles in high yields.Excellent stereospecificity of the fragmentation based on the stereochemical outcome was discussed.Simple stereo-controlled synthetic approach to some insect pheromones is also described.