2186-95-0

Basic information

• Product Name: 4,4′-dimethoxybenzhydryl methyl ether
• Synonyms: 4,4′-dimethoxybenzhydryl methyl ether
• CAS NO: 2186-95-0
• Molecular Weight: 258.317
• Mol File: 2186-95-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 4,4′-dimethoxybenzhydryl methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4′-dimethoxybenzhydryl methyl ether(2186-95-0)
• EPA Substance Registry System: 4,4′-dimethoxybenzhydryl methyl ether(2186-95-0)

Safety Data

• Hazardous Substances Data: 2186-95-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 116664-86-9 bis(4-methoxyphenyl)methyl 4-cyanophenyl ether 
• 728-87-0 4,4'-Dimethoxybenzhydrol 
• 149-73-5 trimethyl orthoformate 
• 7525-23-7 4,4'-dimethoxydiphenylmethyl chloride 
• 69545-37-5 di(p-anisyl)methyl bromide 
• 958-80-5 bis(4-methoxyphenyl)thione 
• 20114-55-0 4,4'-dimethoxybenzophenone hydrazone 
• 132417-64-2 methyl tris(4-methoxyphenyl)acetate 
• 42240-30-2 bis-(4-methoxyphenyl)methyl acetate 
• 124-41-4 sodium methylate 

Downstream Products

• 67-56-1 methanol 
• 42240-30-2 bis-(4-methoxyphenyl)methyl acetate 
• 728-87-0 4,4'-Dimethoxybenzhydrol 

Relevant articles and documents

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Direct and Asymmetric Nickel(II)-Catalyzed Construction of Carbon-Carbon Bonds from N-Acyl Thiazinanethiones

A wide array of new N-acyl thiazinanethiones are employed in a number of direct and enantioselective carbon-carbon-bond-forming reactions catalyzed by nickel(II) complexes. The electrophilic species are mostly prepared in situ from ortho esters, methyl et

Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2

The structurally simple (Me3P)2NiCl2 complex catalyzes SN1-type alkylations of chiral N-acyl thiazolidinethiones with diarylmethyl methyl ethers and other stable carbenium cations. The former can contain a varie