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

• 588-46-5 N-(phenylmethyl)acetamide 
• 2216-69-5 1-Methoxynaphthalene 
• 946-80-5 (benzyloxy)benzene 
• 100-44-7 benzyl chloride 
• 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 
• 90-15-3 α-naphthol 
• 2607-25-2 1-iodo-4-methoxynaphthalene 
• 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

Reductive Coupling between C-N and C-O Electrophiles

The cross-electrophile reaction is a promising strategy for C-C bond formation. Recent studies have focused mainly on reactions with organic halides. Here we report a coupling reaction between C-N and C-O electrophiles that demonstrates the possibility of constructing a C-C bond via C-N and C-O cleavage. Several reactions between benzyl/aryl ammonium salts and vinyl/aryl C-O electrophiles have been studied. Preliminary mechanistic studies revealed that the benzyl ammoniums were activated through a radical mechanism.