125342-95-2

Basic information

• Product Name: 6-methoxy-2-(phenylmethoxy)-1-naphthalenecarboxaldehyde
• Synonyms: 6-methoxy-2-(phenylmethoxy)-1-naphthalenecarboxaldehyde
• CAS NO: 125342-95-2
• Molecular Weight: 292.334
• Mol File: 125342-95-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-methoxy-2-(phenylmethoxy)-1-naphthalenecarboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methoxy-2-(phenylmethoxy)-1-naphthalenecarboxaldehyde(125342-95-2)
• EPA Substance Registry System: 6-methoxy-2-(phenylmethoxy)-1-naphthalenecarboxaldehyde(125342-95-2)

Safety Data

• Hazardous Substances Data: 125342-95-2(Hazardous Substances Data)

Upstream product

• 50493-59-9 2-hydroxy-6-methoxynaphthalene-1-carbaldehyde 
• 100-39-0 benzyl bromide 
• 107-03-9 1-thiopropane 
• 55218-08-1 2,6-dimethoxy-1-naphthalenecarbaldehyde 
• 584-08-7 potassium carbonate 

Downstream Products

• 125342-94-1 N-[[6-Methoxy-2-(phenylmethoxy)-5-(trifluoromethyl)-1-naphthalenyl]carbonyl]-N-methylglycine Methyl Ester 
• 124323-67-7 [(2-Benzyloxy-6-methoxy-5-trifluoromethyl-naphthalene-1-carbothioyl)-methyl-amino]-acetic acid 
• 134057-63-9 [(2-Benzyloxy-6-methoxy-5-trifluoromethyl-naphthalene-1-carbonyl)-methyl-amino]-acetic acid 
• 134057-89-9 2-Benzyloxy-6-methoxy-naphthalene-1-carboxylic acid 

Relevant articles and documents

Synthesis and structure-activity relationships of 2-amino-1- aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents

A series of aroylnaphthalene derivatives were prepared as bioisosteres of combrestatin A-4 and evaluated for anticancer activity. 2-Amino-1- aroylnaphthalene and 2-hydroxy-1-aroylnaphthalene, 9 and 8, respectively, showed strong antiproliferative activity

Production of N-((2-alkoxy-6-methoxy-5-(trifluoromethyl)-1-naphthalenyl)carbonyl)-N-methylglycine esters

Process for the production of N-[[2-alkoxy-6-methoxy-5-(trifluoromethyl)-1-naphthalenyl]carbonyl]-N-methylglycine esters and intermediates for their production. Said esters are themselves intermediates for the manufacture of compounds which inhibit aldose