39863-70-2

Basic information

• Product Name: 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol
• Synonyms: 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol
• CAS NO: 39863-70-2
• Molecular Weight: 194.274
• Mol File: 39863-70-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol(39863-70-2)
• EPA Substance Registry System: 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol(39863-70-2)

Safety Data

• Hazardous Substances Data: 39863-70-2(Hazardous Substances Data)

Upstream product

• 134435-48-6 3-(1-methylethenyl)-4-methoxyphenylethyl acetate 
• 75-21-8 oxirane 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 134435-49-7 1-isopropyl-4-methoxyphenylethyl acetate 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 134435-46-4 3-acetyl-4-methoxyphenylethyl acetate 
• 134435-47-5 3-(1-hydroxy-1-methylethyl)-4-methoxyphenylethanol 
• 702-23-8 2-(4-Methoxyphenyl)ethanol 

Downstream Products

• 100172-08-5 8-(4-Methoxy-3-isopropyl-phenyl)-5-oxo-octansaeure-methylester 
• 128291-67-8 3-(3-isopropyl-4-methoxyphenyl)propionitrile 
• 134435-55-5 2-Benzenesulfinyl-7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 
• 134435-53-3 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 
• 134435-54-4 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-4,4a,10,10a-tetrahydro-1H-phenanthren-9-one 
• 61494-73-3 12-hydroxy-abieta-8,11,13-trien-3,7-dione 
• 134435-51-1 (E)-2-(3-Isopropyl-4-methoxy-phenyl)-5,9-dimethyl-deca-4,8-dienenitrile 
• 64929-62-0 3-isopropyl-4-methoxybenzyl bromide 
• 31859-25-3 4-Methoxy-3-isopropylphenylacetonitrile 
• 31825-29-3 3‐isopropyl‐4‐methoxybenzaldehyde 
• 31816-29-2 4-Methoxy-3-isopropylbenzyl alcohol 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 2944-47-0 o-isopropylanisole 
• 187161-51-9 3-Isopropoxy-6-[2-(3-isopropyl-4-methoxy-phenyl)-ethyl]-5,5-dimethyl-cyclohex-2-enone 

Relevant articles and documents

Total synthesis of (±)-Scrodentoid A

An efficient total synthesis of scrodentoid A was accomplished starting from a Hagemann's ester and a substituted (2-bromoethyl)benzene. Key reactions in this synthesis include C-alkylation of the Hagemann's ester, 6-endo-Trig cationic cyclization of an enone and Lewis acid promoted isomerization of a cis-fused ketone.

Synthesis of aromatic diterpenes synthesis of 12-hydroxy-abieta-8,11,13-trien-3,7-dione

Model studies involving cationic cyclisation of suitable dienes have provided a synthesis of the title compound. Preparation of the dienes from available aromatic starting materials and the modification of the cyclised products are described.