51010-48-1

Basic information

• Product Name: 1-methoxy-4-benzylnaphthalene
• Synonyms: 1-methoxy-4-benzylnaphthalene
• CAS NO: 51010-48-1
• Molecular Weight: 248.324
• Mol File: 51010-48-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-methoxy-4-benzylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-benzylnaphthalene(51010-48-1)
• EPA Substance Registry System: 1-methoxy-4-benzylnaphthalene(51010-48-1)

Safety Data

• Hazardous Substances Data: 51010-48-1(Hazardous Substances Data)

Upstream product

• 2607-25-2 1-iodo-4-methoxynaphthalene 
• 54877-68-8 (4-methoxy-[1]naphthylmethyl)-dimethyl-amine 
• 15971-29-6 4-methoxy-1-naphthaldehyde 
• 16156-59-5 phenyl methanesulfonate 
• 640-60-8 toluene-4-sulfonic acid phenyl ester 
• 17763-67-6 Phenyl triflate 
• 108-95-2 phenol 
• 100-44-7 benzyl chloride 
• 90-15-3 α-naphthol 
• 2216-69-5 1-Methoxynaphthalene 
• 946-80-5 (benzyloxy)benzene 
• 588-46-5 N-(phenylmethyl)acetamide 
• 28178-96-3 4-(phenylmethyl)-1-naphthalenol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 72261-62-2 4-benzylnaphthalene-1,2-dione 
• 28178-96-3 4-(phenylmethyl)-1-naphthalenol 

Relevant articles and documents

Construction of C-C Bond via C-N and C-O Cleavage

The construction of a C-C bond is a center subject in synthetic organic chemistry. The cross-electrophile coupling has provided a powerful tool to forge the C-C bond. However, this process generally requires organic halides, which has severely restricted

Benzylation of Arenes with Benzyl Halides under Promoter-Free and Additive-Free Conditions

It was found that benzyl chlorides and bromides could directly react with electron-rich arenes, which provided an example of promoter-free and additive-free benzylation of arenes. A variety of benzyl chlorides and bromides were treated with benzene rings to give the targeted products in low to high yields. The present conditions tolerated the vinyl group of the substrates. Preliminary mechanistic investigation suggests that the present reactions possibly proceed via an autocatalytic mechanism pathway.