66498-33-7

Basic information

• Product Name: Benzenemethanol, 3-methoxy-4-(1-methylethyl)-
• CAS NO: 66498-33-7
• Molecular Formula: C11H16O2
• Molecular Weight: 180.247
• Mol File: 66498-33-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 3-methoxy-4-(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3-methoxy-4-(1-methylethyl)-(66498-33-7)
• EPA Substance Registry System: Benzenemethanol, 3-methoxy-4-(1-methylethyl)-(66498-33-7)

Safety Data

• Hazardous Substances Data: 66498-33-7(Hazardous Substances Data)

Upstream product

• 77311-68-3 5-(hydroxymethyl)-2-(1-methylethyl)phenol 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 71745-51-2 3-Hydroxy-4-isopropylbenzoesaeuremethylester 
• 19420-59-8 3-hydroxy-4-isopropyl-benzoic acid 
• 1076-56-8 Thymol methyl ether 
• 77878-31-0 7-acetoxymethyl-4-methylcoumarin 
• 59555-33-8 3-acetoxy-4-isopropyl-benzyl acetate 
• 53878-05-0 7-bromomethyl-4-methylcoumarin 
• 66498-32-6 7-acetoxythymol methyl ether 
• 33280-65-8 4-isopropyl-3-methoxy-benzyl isobutyrate 

Downstream Products

• 33280-65-8 4-isopropyl-3-methoxy-benzyl isobutyrate 
• 183122-28-3 4-isopropyl-3-methoxybenzyl bromide 
• 1027946-28-6 6,6-dimethyl-2-(4-isopropyl-3-methoxyphenylmethyl)-3-methoxy-2-cyclohexenone 
• 183122-37-4 4,4-dimethyl-2-(4-isopropyl-3-methoxyphenylmethyl)-3-vinyl-2-cyclohexenone 
• 183122-35-2 4,4-dimethyl-2-(4-isopropyl-3-methoxyphenylmethyl)-1,3-cyclohexanedione 
• 183122-54-5 2-(4-isopropyl-3-methoxyphenylmethyl)-1,3-cyclohexanedione 
• 183122-24-9 2-(3-methoxy-4-isopropylphenylmethyl)-3-vinyl-2-cyclohexenone 
• 183122-55-6 2-(4-isopropyl-3-methoxyphenylmethyl)-3-methoxy-2-cyclohexenone 
• 33280-66-9 3-Methyl-butyric acid 4-isopropyl-3-methoxy-benzyl ester 

Relevant articles and documents

Synthesis of Two Naturally Ocurring Isobutyrates Related to Thymol

7-Acetoxymethylcoumarin (15), prepared by heating 7-bromomethyl-4-methylcoumarin (14) with sodium acetate and acetic acid, on heating with NaOH-ethylene glycol, furnishes 3-hydroxy-4-isopropylbenzyl alcohol (3).Compound (3) has been transformed into diisobutyrate (1) of 3-hydroxy-4-isopropylbenzyl alcohol.Selective methylation of 3 furnishes 4-isopropyl-3-methoxybenzyl alcohol (5), an intermediate for the synthesis of sempervirol.Acylation of 5 gives the naturally ocurring 4-isopropyl-3-methoxybenzyl isobutyrate (2). 4,7-Dimethylcoumarin affords o-isopropenylphenol (7) when heated with aq.NaOH at 140 deg C, but if the reaction is carried out at 210 deg C the product formed is m-cresol (17).