2431-91-6

Basic information

• Product Name: 4-Methoxy-2,6-xylenol
• Synonyms: 4-Methoxy-2,6-dimethylphenol;4-Methoxy-2,6-xylenol;Nsc128407
• CAS NO: 2431-91-6
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.1904
• Mol File: 2431-91-6.mol
• Article Data: 8

Chemical Properties

• Melting Point: 77 °C
• Boiling Point: 263.6°Cat760mmHg
• Flash Point: 130°C
• Appearance: /
• Density: 1.053g/cm³
• PKA: 11.16±0.23(Predicted)
• CAS DataBase Reference: 4-Methoxy-2,6-xylenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methoxy-2,6-xylenol(2431-91-6)
• EPA Substance Registry System: 4-Methoxy-2,6-xylenol(2431-91-6)

Safety Data

• Hazardous Substances Data: 2431-91-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 654-42-2 1,4-dihydroxy-2,6-dimethylbenzene 
• 576-26-1 2.6-dimethylphenol 
• 81123-14-0 2,6-bis[(dimethylamino)methyl]-4-methoxyphenol 
• 527-61-7 2,6-dimethyl-1,4-benzoquinone 
• 3096-63-7 N-(2,6-dimethylphenyl)hydroxylamine 
• 150-76-5 4-methoxy-phenol 
• 21893-97-0 2,6-bis(hydroxymethyl)-4-methoxyphenol 
• 750624-36-3 1,3-dimethyl-2,5-bis-prop-2-ynyloxy-benzene 
• 750624-43-2 3,5-dimethyl-4-prop-2-ynyloxy-phenol 
• 2374-05-2 4-bromo-2,6-dimethyl-phenol 
• 124-41-4 sodium methylate 
• 50-00-0 formaldehyd 
• 50481-12-4 bis(2,6-dimethyl-4-methoxyphenyl)hydroxyborane 

Downstream Products

• 214754-56-0 4-methoxycarbonyl-N-hydroxyphthalimide 
• 15773-13-4 4-Methoxy-2,6-dimethyl-phenoxy-Radikal 
• 2592-95-2 benzotriazol-1-ol 
• 26198-21-0 6-trifluoromethyl-1-hydroxybenzotriazole 
• 26198-26-5 6-methyl-1H-benzo[d][1,2,3]triazol-1-ol 
• 5319-71-1 3-hydroxy-4-oxo-3,4-dihydroquinazoline 
• 28230-32-2 3-hydroxy-3,4-dihydrobenzotriazine-4-one 
• 57197-12-3 4,4-dimethoxy-2,6-dimethylcyclohexa-2,5-dienone 

Relevant articles and documents

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Direct synthesis of anilines and nitrosobenzenes from phenols

A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an ipso-oxidative aromatic substitution (iSOAr) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.

A second-generation total synthesis of (+)-discodermolide: The development of a practical route using solely substrate-based stereocontrol

(Chemical Equation Presented). A novel total synthesis of the complex polyketide (+)-discodermolide, a promising anticancer agent of sponge origin, has been completed in 7.8% overall yield over 24 linear steps, with 35 steps altogether. This second-genera

SYNTHESIS OF DISCODERMOLIDE

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