147167-38-2

Basic information

• Product Name: N-Allyl-N-cyclohexyl-2-methyl-2,3-butadienamid
• Synonyms: N-Allyl-N-cyclohexyl-2-methyl-2,3-butadienamid
• CAS NO: 147167-38-2
• Molecular Weight: 219.327
• Mol File: 147167-38-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-Allyl-N-cyclohexyl-2-methyl-2,3-butadienamid(CAS DataBase Reference)
• NIST Chemistry Reference: N-Allyl-N-cyclohexyl-2-methyl-2,3-butadienamid(147167-38-2)
• EPA Substance Registry System: N-Allyl-N-cyclohexyl-2-methyl-2,3-butadienamid(147167-38-2)

Safety Data

• Hazardous Substances Data: 147167-38-2(Hazardous Substances Data)

Upstream product

• 6628-00-8 N-Allylcyclohexylamin 
• 147167-26-8 2-Methyl-2,3-butadiensaeurechlorid 
• 18913-36-5 2-methyl-butadienoic acid 
• 18913-37-6 methyl 2-methyl-2,3-butadienoate 

Relevant articles and documents

Cycloadditions, XX, Thermally Induced Intramolecular Reactions of 2-Methyl-2,3-butadienamides

The 2-methyl-2,3-butadienamides 4a-m are directly synthesized by the reaction of the corresponding allenic acid chloride 2 with the secondary amines 3.At heating, 4a-j undergo the intramolecular Diels-Alder reaction, by using their ω-standing double bond and the ?-system of the directly bonded phenyl groups or of the "methylenic" bonded arenes of furans.Thereby the tricycles 6a-g (bearing five-membered lactam moieties) and/or the tricycles 7-9 (bearing six-membered lactam moieties) are formed.The influence of the geminal methyl group on the chemoselectivity and on the velocity of the IMDA reactions is investigated.The N-allyl derivatives of 4 (s. 4l and m) form the bicycles 10 by intramolecular -Cycloaddition. Key words: 2-Methyl-2,3-butadienamides, Intramolecular - and -Cycloadditions