358673-06-0

Basic information

• Product Name: 3-[methyl-(naphthalene-2-sulfonyl)-amino]-benzoic acid ethyl ester
• Synonyms: 3-[methyl-(naphthalene-2-sulfonyl)-amino]-benzoic acid ethyl ester
• CAS NO: 358673-06-0
• Molecular Weight: 369.441
• Mol File: 358673-06-0.mol

Chemical Properties

• CAS DataBase Reference: 3-[methyl-(naphthalene-2-sulfonyl)-amino]-benzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[methyl-(naphthalene-2-sulfonyl)-amino]-benzoic acid ethyl ester(358673-06-0)
• EPA Substance Registry System: 3-[methyl-(naphthalene-2-sulfonyl)-amino]-benzoic acid ethyl ester(358673-06-0)

Safety Data

• Hazardous Substances Data: 358673-06-0(Hazardous Substances Data)

Upstream product

• 93-11-8 2-Naphthalenesulfonyl chloride 
• 582-33-2 3-aminobenzoic acid ethyl ester 
• 209173-75-1 ethyl N-(2-naphthalenesulfonyl)-3-aminobenzoate 
• 74-88-4 methyl iodide 

Downstream Products

• 358673-18-4 N-{2-methoxy-5-[1,6,6-tris-(3-{[(2-dimethylamino-ethyl)-methyl-amino]-methyl}-4-methoxy-phenyl)-1,6-bis-(3-methylamino-phenyl)-hexa-2,4-diynyl]-benzyl}-N,N',N'-trimethyl-ethane-1,2-diamine 
• 358673-14-0 C₇₂H₅₆N₂O₁₂S₂ 
• 413620-79-8 2,2,2-trifluoro-N-methyl-N-(3-{1,1,6,6-tetrakis-(3-formyl-4-methoxy-phenyl)-6-[3-(methyl-trifluoroacetyl-amino)-phenyl]-hexa-2,4-diynyl}-phenyl)-acetamide 
• 358673-12-8 C₆₈H₅₆N₂O₈S₂ 
• 358673-16-2 2,2,2-trifluoro-N-methyl-N-(3-{1,1,6,6-tetrakis-(4-methoxy-phenyl)-6-[3-(methyl-trifluoroacetyl-amino)-phenyl]-hexa-2,4-diynyl}-phenyl)-acetamide 
• 550372-00-4 C₄₈H₄₄N₂O₄ 
• 358673-10-6 naphthalene-2-sulfonic acid {3-[1,1-bis-(4-methoxy-phenyl)-prop-2-ynyl]-phenyl}-methyl-amide 
• 358673-08-2 naphthalene-2-sulfonic acid {3-[hydroxy-bis-(4-methoxy-phenyl)-methyl]-phenyl}-methyl-amide 

Relevant articles and documents

Cooperative ratiometric chemosensors: Pinwheel receptors with an integrated fluorescence system

The synthesis and fluorescent properties of a second generation cooperative chemical sensor are described. The sensor has two interacting binding pockets for cooperative recognition of two analytes. Cooperative binding activates a ratiometric fluorescent response via formation of an excimer. Binding was characterized by NMR, absorption, and fluorescence spectroscopy. The advantages of separating the recognition elements from the fluorescent response elements are discussed.