33257-15-7

Basic information

• Product Name: Benzene, 1,2,3-trimethoxy-4-methyl-
• CAS NO: 33257-15-7
• Molecular Formula: C10H14O3
• Molecular Weight: 182.219
• Mol File: 33257-15-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2,3-trimethoxy-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2,3-trimethoxy-4-methyl-(33257-15-7)
• EPA Substance Registry System: Benzene, 1,2,3-trimethoxy-4-methyl-(33257-15-7)

Safety Data

• Hazardous Substances Data: 33257-15-7(Hazardous Substances Data)

Upstream product

• 25245-37-8 1-iodo-2,3,4-trimethoxy-benzene 
• 616-38-6 carbonic acid dimethyl ester 
• 10385-36-1 2,3,4-trimethoxybromobenzene 
• 74-88-4 methyl iodide 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 

Downstream Products

• 58186-27-9 Idebenone 
• 605-94-7 2,3-Dimethoxy-5-methyl-1,4-benzoquinone 
• 129627-08-3 C₈H₈O₉S₂^(2-)*2K⁽¹⁺⁾ 
• 129627-09-4 C₉H₁₁O₆S^(1-)*K⁽¹⁺⁾ 
• 129627-07-2 C₈H₉O₆S^(1-)*K⁽¹⁺⁾ 
• 129627-06-1 C₈H₉O₆S^(1-)*K⁽¹⁺⁾ 
• 52244-30-1 2,6-Dimethoxy-3-methylphenol 
• 39727-82-7 4-methyl ether of 2,3-dimethoxy-5-methylhydroquinone 
• 31776-35-9 2,6-dimethoxy-3-methyl-1,4-benzoquinone 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 
• 88367-27-5 3-Methoxy-6-methylbenzene-1,2-diol 
• 129627-05-0 3-Methoxy-4-methyl-benzene-1,2-diol 
• 3955-29-1 trihydroxytoluene 

Relevant articles and documents

Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum

The volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were collected by use of a closed-loop stripping apparatus (CLSA) and analysed by GC-MS. The main compound class of both species were polysubstituted benzene derivatives. Their structures could only be unambiguously determined by comparison to all isomers with different substitution patterns. The substitution pattern of the main compound from H. griseobrunneum, the new natural product 2,4,5-trimethylanisole, was explainable by a polyketide biosynthesis mechanism that was supported by a feeding experiment with (methyl-2H3)methionine.

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

Ubiquinones and related compounds. XXII. Synthesis of 2,3-dimethoxy-5-methyl-1,4-benzoquinone and its ethylhomologues

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