118088-55-4

Basic information

• Product Name: 2,3-dimethoxy-4-isopropylphenylmethyl alcohol
• Synonyms: 2,3-dimethoxy-4-isopropylphenylmethyl alcohol
• CAS NO: 118088-55-4
• Molecular Weight: 210.273
• Mol File: 118088-55-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3-dimethoxy-4-isopropylphenylmethyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dimethoxy-4-isopropylphenylmethyl alcohol(118088-55-4)
• EPA Substance Registry System: 2,3-dimethoxy-4-isopropylphenylmethyl alcohol(118088-55-4)

Safety Data

• Hazardous Substances Data: 118088-55-4(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 71720-27-9 3-Isopropyl-veratrol 

Downstream Products

• 1035991-96-8 1-isopropyl-2,3-dimethoxy-4-((methoxymethoxy)methyl)benzene 
• 183122-52-3 3-ethoxy-6-(2,3-dimethoxy-4-isopropylphenylmethyl)-6-methyl-2-cyclohexenone 
• 183122-51-2 2-(2,3-dimethoxy-4-isopropylphenylmethyl)-3-methoxy-6-methyl-2-cyclohexenone 
• 183122-17-0 2-(2,3-dimethoxy-4-isopropylphenylmethyl)-3-vinyl-2-cyclohexenone 
• 183122-20-5 4-(2,3-dimethoxy-4-isopropylphenylmethyl)-4-methyl-3-vinyl-2-cyclohexenone 
• 146725-02-2 6,6-dimethyl-2-(2,3-dimethoxy-4-isopropylphenylmethyl)-3-methoxy-2-cyclohexenone 
• 146725-01-1 4,4-dimethyl-2-(2,3-dimethoxy-4-isopropylphenylmethyl)-1,3-cyclohexanedione 
• 146724-98-3 4,4-dimethyl-2-(2,3-dimethoxy,4-isopropylphenylmethyl)-3-vinyl-2-cyclohexenone 
• 183122-15-8 2-(2,3-dimethoxy-4-isopropylphenylmethyl)-3-methoxy-2-cyclohexenone 
• 183122-14-7 2-(2,3-dimethoxy-4-isopropylphenylmethyl)-1,3-cyclohexanedione 
• 1026465-43-9 8-(4-isopropyl-2,3-dimethoxy-benzyl)-6,6-dimethyl-7-vinyl-1,4-dioxa-spiro[4.5]decan-7-ol 
• 182689-73-2 6-(2,3-dimethoxy-4-isopropylbenzyl)-2,2-dimethyl-3,3-ethylenedioxycyclohexanone 
• 110300-77-1 taxamairin B 
• 146725-00-0 2,3-dimethoxy-4-isopropylphenylmethyl bromide 

Relevant articles and documents

The total synthesis of (±)-barbatusol

An eight-step synthesis of the naturally occurring hypotensive diterpene barbatusol (3) featuring a Friedel-Crafts annulation is reported.

Use of conjugated dienones in cyclialkylations: The total syntheses of (±)-barbatusol, (±)-pisiferin, (±)-deoxofaveline, (±)-xochitlolone, and (±)-faveline

Concise syntheses of five tricyclic diterpenoids are reported. The key reaction in each synthesis is a cyclialkylation of a functionalized arene with a Lewis acid-activated conjugated dienone to generate a 6,7,6-fused tricycle.