181259-00-7

Basic information

• Product Name: methyl 8-phenoxy-4-{[(trifluoromethyl)sulfonyl]oxy}naphthalene-2-carboxylate
• Synonyms: methyl 8-phenoxy-4-{[(trifluoromethyl)sulfonyl]oxy}-2-naphthoate; Methyl-8-phenoxy-4-{[(trifluormethyl)sulfonyl]oxy}-2-naphthoat
• CAS NO: 181259-00-7
• Molecular Formula: C₁₉H₁₃F₃O₆S
• Molecular Weight: 426.3631
• Mol File: 181259-00-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 521.032°C at 760 mmHg
• Flash Point: 268.911°C
• Density: 1.453g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: methyl 8-phenoxy-4-{[(trifluoromethyl)sulfonyl]oxy}naphthalene-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 8-phenoxy-4-{[(trifluoromethyl)sulfonyl]oxy}naphthalene-2-carboxylate(181259-00-7)
• EPA Substance Registry System: methyl 8-phenoxy-4-{[(trifluoromethyl)sulfonyl]oxy}naphthalene-2-carboxylate(181259-00-7)

Safety Data

• Hazardous Substances Data: 181259-00-7(Hazardous Substances Data)

Upstream product

• 181258-94-6 4-Acetoxy-8-phenoxy-naphthalene-2-carboxylic acid methyl ester 
• 19434-34-5 2-(phenoxy)benzaldehyde 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 181258-98-0 4-Hydroxy-8-phenoxy-naphthalene-2-carboxylic acid methyl ester 

Downstream Products

• 181259-29-0 (E)-3-{4-[(Methyl-phenethyl-carbamoyl)-methyl]-8-phenoxy-naphthalen-2-yl}-acrylic acid ethyl ester 
• 181259-07-4 4-[(Methyl-phenethyl-carbamoyl)-methyl]-8-phenoxy-naphthalene-2-carboxylic acid methyl ester 
• 181259-27-8 (E)-3-[4-(2-Hydroxy-ethyl)-8-phenoxy-naphthalen-2-yl]-acrylic acid ethyl ester 
• 181259-05-2 4-Carboxymethyl-8-phenoxy-naphthalene-2-carboxylic acid methyl ester 
• 181259-03-0 4-(2-Hydroxy-ethyl)-8-phenoxy-naphthalene-2-carboxylic acid methyl ester 
• 181259-26-7 4-(2-Hydroxy-ethyl)-8-phenoxy-naphthalene-2-carbaldehyde 
• 181259-01-8 8-Phenoxy-4-vinyl-naphthalene-2-carboxylic acid methyl ester 

Relevant articles and documents

Structure-activity relationships study of two series of leukotriene B4 antagonists: Novel indolyl and naphthyl compounds substituted with a 2- [methyl(2-phenethyl)amino]-2-oxoethyl side chain

N-Methyl-N-phenethylphenylacetamide has been reported to be a key binding domain to LTB4 receptors. Here we describe the synthesis and structure-activity relationship (SAR) studies of two new series of LTB4 receptor antagonists in wh