150094-87-4

Basic information

• Product Name: Benzene, 2-(1,1-dimethylethyl)-1-(methoxymethoxy)-4-methyl-
• CAS NO: 150094-87-4
• Molecular Formula: C13H20O2
• Molecular Weight: 208.301
• Mol File: 150094-87-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 2-(1,1-dimethylethyl)-1-(methoxymethoxy)-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-(1,1-dimethylethyl)-1-(methoxymethoxy)-4-methyl-(150094-87-4)
• EPA Substance Registry System: Benzene, 2-(1,1-dimethylethyl)-1-(methoxymethoxy)-4-methyl-(150094-87-4)

Safety Data

• Hazardous Substances Data: 150094-87-4(Hazardous Substances Data)

Upstream product

• 109-87-5 Dimethoxymethane 
• 2409-55-4 2-tert-Butyl-4-methylphenol 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 1027586-11-3 3-tert-Butyl-2-methoxymethoxy-5-methyl-benzoic acid 
• 882500-52-9 3-(tert-butyl)-5-formyl-4-hydroxybenzoic acid 
• 882500-53-0 methyl-3-tert-butyl-5-formyl-4-hydroxybenzoate 
• 39778-63-7 3-(1,1-dimethylethyl)-4-hydroxybenzoic acid methyl ester 
• 66737-88-0 4-hydroxy-3-tert-butyl benzoic acid 
• 4103-77-9 2-(tert-butyl)-6-(methoxymethyl)-4-methylphenol 

Relevant articles and documents

Benzylic C-H trifluoromethylation of phenol derivatives

Phenol derivatives were trifluoromethylated using copper/Togni reagent. In dimethylformamide, the benzylic C-H bond at the para position of the hydroxyl group was selectively substituted with a CF3 group. In contrast, aromatic C-H trifluorometh

A new and efficient conversion of alkylphenols into the corresponding substituted salicylic acids

A three-step sequence suitable for the synthesis of alkyl substituted salicylic acids from the corresponding alkylphenols involves ortho-directed lithiation of the methoxymethyl aryl ethers followed by quenching with carbon dioxide and deprotection under acidic conditions.