22273-94-5

Basic information

• Product Name: Cyclohexanol, 2-(3-hydroxy-1-butenylidene)-1,3,3-trimethyl-
• CAS NO: 22273-94-5
• Molecular Formula: C13H22O2
• Molecular Weight: 210.316
• Mol File: 22273-94-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanol, 2-(3-hydroxy-1-butenylidene)-1,3,3-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 2-(3-hydroxy-1-butenylidene)-1,3,3-trimethyl-(22273-94-5)
• EPA Substance Registry System: Cyclohexanol, 2-(3-hydroxy-1-butenylidene)-1,3,3-trimethyl-(22273-94-5)

Safety Data

• Hazardous Substances Data: 22273-94-5(Hazardous Substances Data)

Upstream product

• 43126-16-5 4-(2,2,6-Trimethylcyclohex-1-en-1-yl)-3-butin-2-yl-acetat 
• 22029-76-1 beta-ionol 

Downstream Products

• 23726-91-2 beta damascone 

Relevant articles and documents

Therapeutic and prophylactic agents for peptic ulcers

A therapeutic and prophylactic agent for peptic ulcers comprising as an effective ingredient a cyclohexane derivative represented by general formula (I): STR1 wherein A represents a group shown by formula, >CH2, STR2 wherein X represents ethynylene, vinylene or ethylene, Y represents oxo or a hydroxy group; R1, R3, R4 and R5 each represents a hydrogen atom or alkyl; R2 represents a hydrogen atom, alkyl or a group shown by --OR8 ; R6 represents a hydrogen atom, oxo or a group shown by --OR8 ; and R7 represents a hydrogen atom or a group shown by --OR8, wherein R8 represents a hydrogen atom or an organic residue.

148. The synthesis of damascenone and β-damascone and the possible mechanism of their formation from carotenoids

A brief synthesis of damascenone (5) from the acetylenic diol 2 and also that of β-damascone (8) from β-ionol, resembling the biogenetic synthesis, are described. A possible mechanism for the formation of damascenone from neoxanthin is proposed.