88367-27-5

Upstream product

• 2103-57-3 2,3,4-trimethoxybenzaldehyde 
• 934-00-9 3-methocycatechol 
• 2144-08-3 2,3,4-trihydroxybenzylaldehyde 
• 77-78-1 dimethyl sulfate 
• 33257-15-7 1,2,3-trimethoxy-4-methylbenzene 
• 4055-69-0 2,3-dihydroxy-4-methoxybenzaldehyde 

Downstream Products

• 88367-28-6 2,3-diacetoxy-4-methoxytoluene 
• 88367-32-2 7-hydroxy-6-methoxy-2-methylbenzo[b]furan 
• 88367-29-7 Acetic acid 2-acetoxy-3-bromomethyl-6-methoxy-phenyl ester 
• 88367-30-0 (2,3-Diacetoxy-4-methoxy-benzyl)-triphenyl-phosphonium; bromide 
• 129627-08-3 C₈H₈O₉S₂^(2-)*2K⁽¹⁺⁾ 
• 129627-06-1 C₈H₉O₆S^(1-)*K⁽¹⁺⁾ 
• 129627-07-2 C₈H₉O₆S^(1-)*K⁽¹⁺⁾ 

Relevant academic research and scientific papers

Stereoelectronic effects on 1H nuclear magnetic resonance chemical shifts in methoxybenzenes

(Graph Presented) Investigation of all O-methyl ethers of 1,2,3-benzenetriol and 4-methyl-1,2,3-benzenetriol (3-16) by 1H NMR spectroscopy and density-functional calculations disclosed practically useful conformational effects on 1H

Isolation and structural elucidation of biotransformation products from acarbose

Following oral administration the α-glucosidase inhibitor acarbose (O-4,6-dideoxy-4-[[1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2- cyclohexen-1-yl]amino]-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl- (1→4)-D-glucopyranose, Bay g 5421) is degraded b

A Simple Synthesis of the Natural Benzofuranoquinone, Acamelin

Acamelin, an allergy-inducing benzofuranoquinone extractive of Australian blackwood has been synthesized from 3-methoxypyrocatechol in six steps.The key step involved formation of a 2-methylbenzofuran by the intramolecular Wittig reaction of an ortho-acet