2675-78-7

Basic information

• Product Name: 2-Chloro-5-methyl-1,4-dimethoxybenzene
• Synonyms: 2-Chloro-5-methyl-1,4-dimethoxybenzene
• CAS NO: 2675-78-7
• Molecular Weight: 186.638
• Mol File: 2675-78-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Chloro-5-methyl-1,4-dimethoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-5-methyl-1,4-dimethoxybenzene(2675-78-7)
• EPA Substance Registry System: 2-Chloro-5-methyl-1,4-dimethoxybenzene(2675-78-7)

Safety Data

• Hazardous Substances Data: 2675-78-7(Hazardous Substances Data)

Upstream product

• 95-71-6 2-methylbenzene-1,4-diol 
• 172655-08-2 2-[(2-Phenylethoxy)methyl]-5-methyl-1,4-dimethoxybenzene 
• 32176-89-9 1,4-Dimethoxy-2-methoxymethyl-5-methyl-benzene 
• 5628-37-5 2,5-Bis(methoxymethyl)-1,4-dimethoxybenzene 
• 50874-27-6 1,4-bis(bromomethyl)-2,5-dimethoxybenzene 
• 65109-51-5 2-(Bromomethyl)-5-methyl-1,4-dimethoxybenzene 
• 24599-58-4 2,5-dimethoxy toluene 
• 3948-92-3 bis(2,5-dimethoxy-4-methylphenyl)methane 
• 118-52-5 1,3-dichloro-5,5-dimethylhydantoin 

Downstream Products

• 124010-13-5 1-(bromomethyl)-4-chloro-2,5-dimethoxybenzene 
• 124010-11-3 Ethyl 4-(acetyloxy)-6-chloro-5,8-dimethoxy-2-naphthalenecarboxylate 
• 124010-10-2 3-Carbethoxy-4-(4-chloro-2,5-dimethoxyphenyl)-3-butenoic acid 
• 90064-48-5 4-chloro-2,5-dimethoxybenzaldehyde 

Relevant articles and documents

Radical-Cation Catalysis in the Synthesis of Diphenylmethanes via the Dealkylative Coupling of Benzylic Ethers

The dealkylative coupling of benzyl alkyl ethers (ArCH2OR) to yield the corresponding diarylmethanes (ArCH2Ar) together with dialkoxymethane (ROCH2OR) is catalyzed by small amounts of 1-electron oxidants (such as aromatic cation radicals, NO(1+), etc.) or by an equivalent electrochemical (anodic) method.The catalytic method is successfully employed for the facile synthesis of a novel macrocyclic crown ether 18 that contains a diarylmethane linkage.On the basis of the spectral observation of the radical cation ArCH2OR.+ and the excellent catalytic efficiency with turnover numbers in excess of 1E2, an electron-transfer and an alternative electrophilic chain mechanism are discussed for the dealkylative coupling process.