35355-33-0

Basic information

• Product Name: 4-METHOXY-2,3-DIMETHYL-PHENOL
• Synonyms: 4-METHOXY-2,3-DIMETHYL-PHENOL
• CAS NO: 35355-33-0
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.19038
• Mol File: 35355-33-0.mol

Chemical Properties

• Boiling Point: 266.668°C at 760 mmHg
• Flash Point: 133.784°C
• Appearance: /
• Density: 1.054g/cm³
• Vapor Pressure: 0.005mmHg at 25°C
• Refractive Index: 1.528
• CAS DataBase Reference: 4-METHOXY-2,3-DIMETHYL-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXY-2,3-DIMETHYL-PHENOL(35355-33-0)
• EPA Substance Registry System: 4-METHOXY-2,3-DIMETHYL-PHENOL(35355-33-0)

Safety Data

• Hazardous Substances Data: 35355-33-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H12O2/c1-6-7(2)9(11-3)5-4-8(6)10/h4-5,10H,1-3H3

Upstream product

• 67-56-1 methanol 
• 608-43-5 2,3-dimethyl-1,4-dihydroxybenzene 
• 38998-17-3 2,3-dimethyl-4-methoxybenzaldehyde 
• 3096-69-3 4-amino-2,3-dimethylphenol 
• 2944-49-2 2,3-dimethylanisole 
• 526-86-3 2,3-dimethyl-1,4-benzoquinone 
• 526-75-0 2,3-Dimethylphenol 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 141989-00-6 2,3-dimethyl-6-(hydroxymethyl)-4-methoxyphenol 
• 35355-34-1 1-(2,2-Diethoxy-ethoxy)-4-methoxy-2,3-dimethyl-benzene 
• 885703-25-3 (S,S)-4-(4-methoxy-2,3-dimethylphenoxy)hexa-1,5-dien-3-ol 
• 38998-19-5 6-Allyl-4-methoxy-2,3-dimethyl-phenol 
• 39021-85-7 1-Allyl-2,5-dimethoxy-3,4-dimethyl-benzene 
• 141989-02-8 6-(t-butyldimethylsilyloxy)methyl-4,4-dimethoxy-2,3-dimethyl-2,5-cyclohexadienone 
• 141989-01-7 6-(t-butyldimethylsilyloxy)methyl-2,3-dimethyl-4-methoxyphenol 
• 885703-27-5 (S,S)-4-(4-methoxy-2,3-dimethylphenoxy)hexa-1,5-dien-3-yl acrylate 
• 885703-28-6 (S,S)-5-(1-(4-methoxy-2,3-dimethylphenoxy)allyl)furan-2(5H)-one 
• 141988-93-4 4,4-dimethoxy-2,3-dimethyl-p-benzoquinone monoketal 

Relevant articles and documents

Substituent effect on the photochemistry of 4,4-dialkoxylated- and 4-hydroxylated cyclohexenones

Photochemistry of the title compounds in various solvents was studied using a broad band of light centered at 350 nm. C-4 spiroketal cyclohexenone 4 (1.0 M) afforded dimers and 12b with the predominance of the former in polar solvent and the latter in non

Efficient and green telescoped process to 2-methoxy-3-methyl-[1,4] benzoquinone

A telescoped process for the preparation of 2-methoxy-3-methyl-[1,4] benzoquinone is disclosed. When this novel process is compared to the prevailing method that utilizes Na2Cr2O7 as the oxidant, the novel process represen

Formal syntheses of (±)-methylenomycins A and B

The syntheses of methyl ester of (±)-desepoxy-4,5-didehydromethylenomycin A (4) and 2,3-dimethyl-5-methoxycarbonyl-2-cyclopentenone (5) were accomplished from a common starting material, 2,3-dimethyl-4-methoxyphenol (8), in only four and two steps in 35%

The Baeyer-Villiger Oxidation of Aromatic Aldehydes and Ketones with Hydrogen Peroxide Catalyzed by Selenium Compounds

A series of organoselenium compounds was investigated as activators of hydrogen peroxide in the Baeyer-Villiger oxidation.As a result, a convenient and cheap method for transformation of aromatic aldehydes, having polycondensed ring systems or electron-donating substituents, and polymethoxy derivatives of acetophenone, into phenols was elaborated.This method utilizes hydrogen peroxide activated by areneseleninic acids, as oxidizing agent.