75445-61-3

Basic information

• Product Name: 1,4-Naphthalenedione, 5-(phenylmethoxy)-
• CAS NO: 75445-61-3
• Molecular Formula: C17H12O3
• Molecular Weight: 264.28
• Mol File: 75445-61-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,4-Naphthalenedione, 5-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Naphthalenedione, 5-(phenylmethoxy)-(75445-61-3)
• EPA Substance Registry System: 1,4-Naphthalenedione, 5-(phenylmethoxy)-(75445-61-3)

Safety Data

• Hazardous Substances Data: 75445-61-3(Hazardous Substances Data)

Upstream product

• 83-56-7 1,5-dihydroxynaphthalene 
• 481-39-0 5-hydroxynaphtho-1,4-quinone 
• 100-44-7 benzyl chloride 
• 620-05-3 iodomethylbenzene 
• 100-39-0 benzyl bromide 

Downstream Products

• 112776-88-2 8-Benzyloxy-9,10-dioxo-1,4,4a,9,9a,10-hexahydro-anthracene-1-carboxylic acid 
• 112776-87-1 5-Benzyloxy-9,10-dioxo-1,4,4a,9,9a,10-hexahydro-anthracene-1-carboxylic acid 
• 126922-34-7 1,4-dihydro-4,4-dimethoxy-8-benzyloxy-napthalen-1-one 
• 1607448-13-4 C₃₄H₂₅NO₃ 
• 1607447-85-7 8-(benzyloxy)-2-(propylamino)naphthalene-1,4-dione 
• 1403498-19-0 5-benzyloxy-1,4,4a,9a-tetrahydro-1,4-ethano-9,10-anthraquinone 
• 1403498-18-9 5-benzyloxy-1,4,4a,9a-tetrahydro-1,4-methano-9,10-anthraquinone 
• 114862-75-8 8-ethyl-10,12-dimethoxy-1-(phenylmethoxy)-6H-benzonaphtho<1,2-b>pyran-6-one 
• 133344-07-7 5-Ethyl-2-iodo-3-methoxy-benzoic acid 5-benzyloxy-4-methoxy-naphthalen-1-yl ester 
• 119650-51-0 1-benzyloxy-10,12-dimethoxy-8-methyl-6H-benzo[d]naphtho[1,2-b]pyran-6-one 
• 133344-06-6 5-(benzyloxy)-4-methoxynaphthalen-1-yl 2-iodo-3-methoxy-5-methylbenzoate 
• 133344-00-0 2-Bromo-benzoic acid 5-benzyloxy-4-methoxy-naphthalen-1-yl ester 
• 133344-01-1 1-Benzyloxy-12-methoxy-dibenzo[c,h]chromen-6-one 
• 133343-99-4 Acetic acid 5-benzyloxy-4-methoxy-naphthalen-1-yl ester 

Relevant articles and documents

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Enantioselective Total Synthesis of (?)-Spiroxins A, C, and D

Spiroxins A, C, and D are metabolites that have been identified in the marine fungal strain LL-37H248. Their unique polycyclic structures and intriguing biological activities make them attractive targets for the synthetic community. Based on a scalable en

Enzymatic desymmetrization/resolution of epoxydiols derived from 1,4-naphthoquinone, 5-hydroxy-1,4-naphthoquinone and 5,8-dihydroxy-1,4- naphthoquinone

The enzymatic desymmetrization/resolution of epoxydiols generated from the basic epoxidation and reduction of 1,4-naphthoquoinone, 5-hydroxy-1,4- naphthoquinone and 5,8-dihydroxy-1,4-naphthoquinone is described. 2,3-Epoxy-1α,2α,3α,4 α-tetrahydronaphthalene-1,4-diol and 5,8-diallyloxy-2,3-epoxy- 1α,2α,3α,4 α-tetrahydronaphthalene-1,4-diol were desymmetrized in the presence of isopropenyl acetate using Burholderia cepacia lipase and Candida antartica lipase B, respectively. An enzymatic resolution of 8-benzyloxy-2,3-epoxy-1α,2α,3 α,4α-tetrahydronaphthalene-1,4-diol using B. cepacia lipase in isopropenyl acetate is also described.