133344-06-6

Basic information

• Product Name: 5-(benzyloxy)-4-methoxynaphthalen-1-yl 2-iodo-3-methoxy-5-methylbenzoate
• Synonyms: 5-(benzyloxy)-4-methoxynaphthalen-1-yl 2-iodo-3-methoxy-5-methylbenzoate
• CAS NO: 133344-06-6
• Molecular Weight: 554.381
• Mol File: 133344-06-6.mol

Chemical Properties

• CAS DataBase Reference: 5-(benzyloxy)-4-methoxynaphthalen-1-yl 2-iodo-3-methoxy-5-methylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(benzyloxy)-4-methoxynaphthalen-1-yl 2-iodo-3-methoxy-5-methylbenzoate(133344-06-6)
• EPA Substance Registry System: 5-(benzyloxy)-4-methoxynaphthalen-1-yl 2-iodo-3-methoxy-5-methylbenzoate(133344-06-6)

Safety Data

• Hazardous Substances Data: 133344-06-6(Hazardous Substances Data)

Upstream product

• 75445-67-9 5-benzyloxy-4-methoxy-1-naphthalenol 
• 140201-79-2 2-iodo-3-methoxy-5-methylbenzoyl chloride 
• 133343-99-4 Acetic acid 5-benzyloxy-4-methoxy-naphthalen-1-yl ester 
• 104506-17-4 4-Acetoxy-8-benzyloxy-1-hydroxynaphthalene 
• 133344-02-2 2-iodo-3-methoxy-5-methylbenzoic acid 
• 119650-46-3 2-Iodo-3-methoxy-5-methyl-benzoic acid methyl ester 
• 108593-44-8 methyl 3-methoxy-5-methylbenzoate 
• 75445-61-3 5-(benzyloxy)-1,4-dihydronaphthalene-1,4-dione 

Downstream Products

• 119650-51-0 1-benzyloxy-10,12-dimethoxy-8-methyl-6H-benzo[d]naphtho[1,2-b]pyran-6-one 

Relevant articles and documents

A xanthate-based free radical approach to defucogilvocarcin M

A formal total synthesis of the aglycon of gilvocarcin M is described. The synthesis is based on the construction of the key naphthalene 7 via a free radical addition-cyclization protocol followed by aromatization of the resulting α-tetralone. This highly

A concise total synthesis of the aglycone of the gilvocarcins

A brief and convergent synthesis of the aglycone of the gilvocarcins M and E (and formally V) involving, in the key step, a Pd-mediated intramolecular biaryl coupling, is reported.