4537-09-1

Basic information

• Product Name: Benzene, 1,4-dimethoxy-2,3,5-trimethyl-
• CAS NO: 4537-09-1
• Molecular Formula: C11H16O2
• Molecular Weight: 180.247
• Mol File: 4537-09-1.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: Benzene, 1,4-dimethoxy-2,3,5-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,4-dimethoxy-2,3,5-trimethyl-(4537-09-1)
• EPA Substance Registry System: Benzene, 1,4-dimethoxy-2,3,5-trimethyl-(4537-09-1)

Safety Data

• Hazardous Substances Data: 4537-09-1(Hazardous Substances Data)

Upstream product

• 700-13-0 Trimethylhydroquinone 
• 77-78-1 dimethyl sulfate 
• 1125-21-9 2,6,6-trimethyl-2-cyclohexene-1,4-dione 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 935-92-2 2,3,5-Trimethyl-1,4-benzoquinone 
• 79-21-0 peracetic acid 
• 496-78-6 2,4,5-trimethylphenol 
• 74-88-4 methyl iodide 

Downstream Products

• 72205-69-7 1,1,4,4-Tetramethoxy-2,3,5-trimethyl-2,5-cyclohexadiene 
• 935-92-2 2,3,5-Trimethyl-1,4-benzoquinone 
• 69821-05-2 1-bromo-2,5-dimethoxy-3,4,6-trimethylbenzene 
• 24891-96-1 trimethyl-nitro-[1,4]benzoquinone 
• 861356-37-8 (2,5-dimethoxy-3,4,6-trimethyl-benzylidene)-malonic acid 
• 87541-38-6 (2,5-dimethoxy-3,4,6-trimethyl-phenyl)-acetonitrile 
• 500886-73-7 (2,5-dimethoxy-3,4,6-trimethyl-phenyl)-acetic acid 
• 150556-43-7 2,5-dimethoxy-3,4,6-trimethylphenol 
• 946860-88-4 C₁₂H₁₆Cl₂O₂ 
• 54757-17-4 1-chloromethyl-2,5-dimethoxy-3,4,6-trimethyl-benzene 
• 700-13-0 Trimethylhydroquinone 
• 103808-42-0 2,5-dimethoxy-3,4,6-trimethylbenzaldehyde 
• 112665-43-7 seratrodast 
• 84071-98-7 1-(2-bromoethyl)-2,5-dimethoxy-3,4,6-trimethylbenzene 

Relevant articles and documents

An ether-linked halogenated phenazine-quinone prodrug model for antibacterial applications

Antibiotic-resistant infections present significant challenges to patients. As a result, there is considerable need for new antibacterial therapies that eradicate pathogenic bacteria through non-conventional mechanisms. Our group has identified a series o

Preparation method of trimethylhydroquinone

The invention discloses a preparation method of trimethylhydroquinone. The preparation method is characterized in that isophorone is used as an initial raw material and oxidized into oxoisophorone, then an acylation reaction occurs in the oxoisophorone and an acylating agent to produce trimethyl hydroquinone diester, and the trimethyl hydroquinone diester is hydrolyzed to produce 2,3,5-trimethylhydroquinone. The method disclosed by the invention has cheap and easily-available raw materials and simple syntheses steps, a used solvent is easy to recover and reuse, and the method needs not use ofa big amount of acid and alkali, thereby reducing pollution of the environment, being convenient for large-scale industrial production and having good application prospects.

Catalytic Asymmetric Cycloadditions of Silyl Nitronates Bearing α-Aryl Group

1,3-Dipolar cycloadditions of 2-alkylacroleins or atropaldehyde with triisopropylsilyl nitronates bearing an α-aryl group produced 3-aryl-2-isoxazolines having a chiral quaternary center in up to 94% ee and up to 88% yield with the aid of Corey’s oxazaborolidine catalyst. Specifically, the TIPS nitronate with an α-(p-methoxyphenyl) group gave mainly the 2-isoxazolines having an all-carbon quaternary center.