18612-99-2

Basic information

• Product Name: Phenol, 5-methyl-2-(1-methylethenyl)-
• CAS NO: 18612-99-2
• Molecular Formula: C10H12O
• Molecular Weight: 148.205
• Mol File: 18612-99-2.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Phenol, 5-methyl-2-(1-methylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 5-methyl-2-(1-methylethenyl)-(18612-99-2)
• EPA Substance Registry System: Phenol, 5-methyl-2-(1-methylethenyl)-(18612-99-2)

Safety Data

• Hazardous Substances Data: 18612-99-2(Hazardous Substances Data)

Upstream product

• 5419-54-5 2,2-bis(2'-hydroxy-4'-methylphenyl)propane 
• 102654-22-8 isopropenyl-m-tolyl ether 
• 108-39-4 3-methyl-phenol 
• 107-18-6 allyl alcohol 
• 107-05-1 3-chloroprop-1-ene 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 
• 14002-90-5 4,7-dimethyl-coumarin 
• 557-31-3 3-ethoxyprop-1-ene 
• 7664-93-9 sulfuric acid 
• 557-40-4 Allyl ether 
• 591-87-7 Allyl acetate 
• 64-19-7 acetic acid 
• 6921-64-8 4'-hydroxy-2'-methylacetophenone 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Downstream Products

• 89-78-1 menthol 
• 89-83-8 thymol 
• 437650-87-8 2-(2-isopropenyl-5-methyl-phenoxy)-2-methyl-propionic acid 
• 437650-89-0 2-methyl-2-(2'-isopropenyl-5'-methyl phenoxy)propan-1-ol 
• 437650-88-9 methyl 2-methyl-2-(2'-isopropenyl-5'-methyl)phenoxy-propionate 
• 138629-69-3 2-(2-isopropenyl-5-methylphenoxy)butanoic acid methyl ester 
• 123870-50-8 ethyl α-(2-hydroxyisopropenyl-5-methyl phenoxy) propionate 
• 64298-14-2 2-(2'-Acetoxy-4'-methylphenyl)-prop-2-enal 
• 14002-90-5 4,7-dimethyl-coumarin 
• 61955-74-6 2-acetoxy-4-methyl-1-(2-methyl-oxiranyl)-benzene 
• 61955-75-7 2-(2-Hydroxy-4-methyl-phenyl)-prop-1-enyl-acetat 
• 152500-90-8 Ethyl 2-(2-isopropenyl-5-methylphenoxy)pent-4-enoate 
• 123870-46-2 2-(2-isopropenyl-5-methylphenoxy)propanoic chloride 
• 740795-73-7 4-(1-aminomethyl-vinyl)-3-methyl-phenol 

Relevant articles and documents

A novel route to thymol from m-cresol

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Total Synthesis of a Dimeric Thymol Derivative Isolated from Arnica sachalinensis

The total synthesis of a dimeric thymol derivative (thymarnicol) isolated from Arnica sachalinensis was accomplished in 6 steps. A key biomimetic Diels–Alder dimerization was found to occur at ambient temperature and the final oxidative cyclization occurs

Ethylene glycol as hydrogen donor for the syntheses of thymol analogues via hydrolysis of 4-methylcoumarins

Treatment of 4-methylcoumarins with potassium hydroxide in ethylene glycol resulted in the formation of the 'normal' 2-isopropenylphenols and/or the 'abnormal' 2-isopropylphenols depending on the nature of the substrates. The solvent ethylene glycol was b