66248-70-2

Basic information

• Product Name: α,2,3,6-Tetramethylbenzene-1-propanol
• Synonyms: α,2,3,6-Tetramethylbenzene-1-propanol
• CAS NO: 66248-70-2
• Molecular Formula: C₁₃H₂₀O
• Molecular Weight: 192.2973
• Mol File: 66248-70-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: α,2,3,6-Tetramethylbenzene-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: α,2,3,6-Tetramethylbenzene-1-propanol(66248-70-2)
• EPA Substance Registry System: α,2,3,6-Tetramethylbenzene-1-propanol(66248-70-2)

Safety Data

• Hazardous Substances Data: 66248-70-2(Hazardous Substances Data)

Upstream product

• 124211-43-4 4-(2-Hydroxymethyl-3,6-dimethyl-phenyl)-butan-2-ol 
• 67-64-1 acetone 
• 917-64-6 methyl magnesium iodide 
• 66248-69-9 3-(2',3',5'-Trimethylphenyl)propanal-1 
• 30316-18-8 1,2-dihydro-3,5,8-trimethyl-naphthalene 
• 124211-42-3 4-(3,6-dimethyl-2-formylphenyl)butan-2-one 
• 76964-13-1 2-formyl-3,4-dihydro-5,8-dimethylnaphthalene 
• 14108-89-5 5,8-dimethyl-1,2-tetrahydronaphthalene 
• 66248-68-8 3-(2',3',5'-Trimethylphenyl)propanol-1 
• 66248-67-7 2-(3'-Propanol-1')-3,6-dimethylbenzyl-alkohol 
• 66248-66-6 2-(3'-Propanol-1')-3,6-dimethylbenzaldehyd 
• 66248-64-4 5,8-Dimethyltetralone-p-toluenesulphonylhydrazone 
• 35044-57-6 ethyl 2,6,6-trimethyl-2,4-cyclohexadiene-1-carboxylate 
• 70429-47-9 5-Hydroxy-2,6,6-trimethyl-2-cyclohexencarbonsaeure-ethylester 

Downstream Products

• 58720-40-4 4-(2,3,6-trimethyl-phenyl)-butan-2-one 
• 2529-36-4 2,3,6-trimethylbenzoic acid 
• 59700-21-9 methyl-3 (trimethyl-2,3,6 phenyl)-5 pentene-1 ol-3 
• 34341-29-2 2,3,6-trimethylbenzaldehyde 
• 57461-21-9 (3E)-4-(2,3,6-trimethylphenyl)but-3-en-2-one 
• 124211-41-2 5-(2,3,6-trimethylphenyl)-3-methylpenta-1,4-dien-3-ol 
• 124211-40-1 4-(2,3,6-trimethylphenyl)-3-bromobutan-2-one 

Relevant articles and documents

A new synthesis of 4-(2,3,6-trimethylphenyl)butan-2-ol, a C13-norisoprenoid artifact from Vitis vinifera linn. and its conversion to several terpenic natural products of plant and marine origin

The four-step synthesis of 4-(2,3,6-trimethylphenyl)butan-2-ol (1), starts from 5,8-dimethyl-3,4-dihydro-2-naphthaldehyde (2).The trimethyldihydronaphthalene (10) obtained from the reduction of 2 is ozonised to the keto aldehyde (11), which is reduced to