109972-84-1

Basic information

• Product Name: 1-Naphthalenol, 5-(phenylmethoxy)-
• CAS NO: 109972-84-1
• Molecular Formula: C17H14O2
• Molecular Weight: 250.297
• Mol File: 109972-84-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenol, 5-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol, 5-(phenylmethoxy)-(109972-84-1)
• EPA Substance Registry System: 1-Naphthalenol, 5-(phenylmethoxy)-(109972-84-1)

Safety Data

• Hazardous Substances Data: 109972-84-1(Hazardous Substances Data)

Upstream product

• 83-56-7 1,5-dihydroxynaphthalene 
• 100-39-0 benzyl bromide 
• 221461-63-8 acetic acid 5-benzyloxy-naphthalen-1-yl ester 
• 690232-00-9 1-benzyl-5-methoxynaphthalene 
• 3588-80-5 5-methoxynaphthalen-1-ol 
• 33892-75-0 5-Methoxy-1-tetralone 
• 605-89-0 1,5-diacetoxynaphthalene 

Downstream Products

• 148914-36-7 5-Benzyloxy-2-bromo-naphthalen-1-ol 
• 888733-65-1 2-(5-(benzyloxy)naphthalen-1-yloxy)acetonitrile 
• 956037-21-1 trifluoromethanesulfonic acid 5-benzyloxynaphthalen-1-yl ester 
• 457049-23-9 5-(benzyloxy)-1,4-dimethoxynaphthalene-2-propanoic acid 
• 457049-22-8 ethyl 5-(benzyloxy)-1,4-dihydro-1,4-dioxonaphthalene-2-propanoate 
• 457049-20-6 ethyl 5-(benzyloxy)-1-hydroxynaphthalene-2-propanoate 
• 776332-18-4 C₄₆H₄₄O₈ 
• 776332-17-3 C₃₂H₃₀O₅ 
• 860615-03-8 C₃₆H₃₈O₇ 
• 776332-16-2 1-benzyloxy-5-[2-(2-bromo-ethoxy)-ethoxy]-naphthalene 
• 457049-19-3 7-(benzyloxy)-2,2-diethoxy-3,4-dihydro-2H-naphtho[1,2-b]pyran 
• 166941-78-2 5-Benzyloxy-2-((2R,4R,5R,6R)-4,5-bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-naphthalen-1-ol 
• 172418-66-5 1-<2-<2-(p-tolylsulfonyl)ethoxy>ethoxy>-5-benzyloxynaphthalene 
• 172418-65-4 1-benzyloxy-5-<2-(2-hydroxyethoxy)ethoxy>naphthalene 

Relevant articles and documents

Towards a Molecular Abacus

The solid state and solution structures of the 1:1 complex formed between the cyclobis(paraquat-p-phenylene) tetracationic cyclophane and 1,5-dimethoxynaphthalene has led to the successful design and characterisation by X-ray crystallography of a prototyp

Anion induced displacement studies in naphthalene diimide containing interpenetrated and interlocked structures

This article describes investigations into the development of supramolecular systems capable of sensing anions through either displacement type assays or molecular motion. An electron deficient naphthalene diimide thread and an electron rich isophthalamid

Synthetic studies on kinamycin antibiotics: Synthesis of a trioxygenated benz[f]indenone and its Diels-Alder reaction to a kinamycin skeleton

A benzo[b]fluorene skeleton such as 10, a basic four-ring system in the revised diazo structures 3 of kinamycin antibiotics, was synthesized by Diels-Alder reaction between dienophile 4,7,8-trioxygenated 1H-benz[f]inden-1-one 11 and Danishefsky-type diene 7. The indenone 11 was prepared by deoxygenation of 2,3-dihydro-1H-benz[f]inden-1-one 12 with the inexpensive 1 -hydroxy-1.2-benziodoxol-3(1H)-one 1-oxide (IBX) after modification of the known protocol. Indenone 12 in turn was obtained from naphthalene-1,5-diol (14) via an intramolecular Friedel-Crafts cyclization of naphthalene-2-propanoic acid 13 as a key step.