6745-75-1

Usage

Uses

2,5-Dimethyl-4-methoxybenzaldehyde may be used in chemical synthesis studies.

InChI:InChI=1/C19H15NO6S2/c21-19(22)14-9-11-15(12-10-14)20-28(25,26)18-8-4-7-17(13-18)27(23,24)16-5-2-1-3-6-16/h1-13,20H,(H,21,22)/p-1

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 1706-11-2 2,5-Dimethyl-anisol 
• 85231-15-8 4-formyl-2,5-dimethylphenol 
• 77-78-1 dimethyl sulfate 
• 67-66-3 chloroform 
• 10028-15-6 ozone 
• 95-87-4 2,5-Dimethylphenol 
• 95-78-3 2,5-Dimethylaniline 
• 74-88-4 methyl iodide 

Downstream Products

• 151539-38-7 4-methoxy-2.5-dimethyl-trans-cinnamic acid 
• 4962-28-1 2,5-dimethyl-4-methoxyphenol 
• 58106-26-6 4-methoxy-2,5-dimethylbenzoic acid 
• 21573-38-6 1-methoxy-2,4,5-trimethylbenzene 
• 98447-19-9 (E)-1-methoxy-2,5-dimethyl-4-(2-nitrovinyl)benzene 
• 84452-11-9 1-Dichloromethyl-4-methoxy-2,5-dimethyl-benzene 
• 68827-86-1 C₃₀H₂₆O₃ 
• 64400-49-3 4-methoxy-2,5-dimethylbenzonitrile 
• 288310-76-9 ethyl 2,5-dimethyl-4-methoxycinnamate 
• 496-78-6 2,4,5-trimethylphenol 
• 3238-38-8 isodurenol 
• 780771-26-8 2,3,4,6-tetramethyl-anisole 
• 722495-58-1 2-methoxy-3,5,6-trimethyl-benzaldehyde 
• 279693-84-4 2,5-dimethyl-4-methoxybenzoyl chloride 

Relevant academic research and scientific papers

TETRAHYDROISOQUINOLINE DERIVATIVES

Compounds of Formula (I) are disclosed and methods of treating viral infections with compositions comprising such compounds.

Process for nucleophilic fluoroalkylation of aldehydes

Aryl difluoromethyl sulfone adds to alkehydes under phase transfer conditions to give novel substituted alcohols of the general formula wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.