53941-13-2

Basic information

• Product Name: (E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene
• Synonyms: (E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene
• CAS NO: 53941-13-2
• Molecular Weight: 178.318
• Mol File: 53941-13-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene(53941-13-2)
• EPA Substance Registry System: (E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene(53941-13-2)

Safety Data

• Hazardous Substances Data: 53941-13-2(Hazardous Substances Data)

Upstream product

• 31089-73-3 1-(2',6',6'-trimethyl-1'-cyclohexenyl)-3-buten-1-one 
• 497-19-8 sodium carbonate 
• 79-77-6 4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one 
• 17283-81-7 4-(2,6,6-Trimethyl-cyclohex-1-enyl)-butan-2-on 
• 53319-91-8 (E)-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-yl acetate 
• 53941-08-5 trans-β-ionone p-tosylhydrazone 
• 446293-91-0 4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol 

Downstream Products

• 23696-85-7 1-(2,6,6-trimethyl-1,3-cyclohexadiene-1-yl)-2-butene-1-one 

Relevant articles and documents

Industrial manufacturing method of damascenone

The invention provides an industrial manufacturing method of damascenone. The industrial manufacturing method is characterized in that damascenone is obtained by oxidizing a compound A. The structural formula of the compound A is shown in the description. The production process and the synthesis route are optimized, in the production course, fewer side reactions are generated, aftertreatment is convenient, production conditions are mild, and the industrial manufacturing method is suitable for industrial production modes.

Reductive displacement of allylic acetates by hydride transfer via catalytic activation by palladium(0) complexes

Allylic acetates are reduced to alkenes by reductive displacement by hydride reagents via catalytic activation with Pd(0) complexes. In the absence of hydrides, allylic acetates afford conjugated dienes in DMSO solvent.