497145-46-7

Basic information

• Product Name: 4-(6-{2-[3-methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-ethylamino}-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-ylmethyl)-benzoic acid tert-butyl ester
• Synonyms: 4-(6-{2-[3-methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-ethylamino}-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-ylmethyl)-benzoic acid tert-butyl ester
• CAS NO: 497145-46-7
• Molecular Weight: 753.893
• Mol File: 497145-46-7.mol

Chemical Properties

• CAS DataBase Reference: 4-(6-{2-[3-methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-ethylamino}-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-ylmethyl)-benzoic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(6-{2-[3-methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-ethylamino}-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-ylmethyl)-benzoic acid tert-butyl ester(497145-46-7)
• EPA Substance Registry System: 4-(6-{2-[3-methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-ethylamino}-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-ylmethyl)-benzoic acid tert-butyl ester(497145-46-7)

Safety Data

• Hazardous Substances Data: 497145-46-7(Hazardous Substances Data)

Upstream product

• 56-91-7 p-aminomethylbenzoic acid 
• 28005-76-7 2-[2-hydroxyethyl-(2-methoxyphenyl)amino]ethanol 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 
• 869634-78-6 [(methoxycarbonylmethyl)(2-methoxyphenyl)amino]-acetic acid methyl ester 
• 107045-28-3 4-(aminomethyl)benzoic acid tert-butyl ester 
• 55696-50-9 tert-butyl 4-cyanobenzoate 
• 619-65-8 4-cyanobenzoic Acid 
• 90-04-0 2-methoxy-phenylamine 
• 19249-03-7 triethylene glycol di-(p-toluenesulfonate) 
• 216852-15-2 4-chloro-N-(4-carboxyphenylmethyl)-1,8-naphthalimide 
• 216852-10-7 N-(4-formyl-2-methoxyphenyl)aza[15]crown-5 ether 
• 98269-22-8 13-(2-methoxyphenyl)-1,4,7,10-tetraoxa-13-cyclopentadecane 
• 4053-08-1 p-chloro-1,8-naphthalicanhydride 
• 497145-43-4 2-[3-methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-ethylamine 

Relevant articles and documents

Preparation method of Na molecular fluorescent intermediate and preparation method of Na molecular fluorescent sensor

The invention provides a preparation method of a Na molecular fluorescent intermediate and a preparation method of a Na molecular fluorescent sensor. The Na molecular fluorescent intermediatehas a structure as shown in a formula I. The preparation method of the Na molecular fluorescent intermediate comprises the following steps: S1, carrying out a substitution reaction on o-anisidineand alpha-methyl haloacetate to obtain a compound 2; S2, carrying out a reduction reaction on the compound 2 to obtain a compound 3; S3, carrying out a hydroxyl substitution on the compound 4 by adopting toluene sulfonyl chloride to obtain a compound 5, wherein the compound 4 has a structural formula as the follows; S4, carrying out a cyclization reaction on the compound 3 and the compound 5 to obtain a compound 6; S5, carrying out a formylation reaction on the compound 6 to obtain a compound 7; S6, carrying out a henry reaction on the compound 7 with nitromethane to obtain a compound 8; and S7, carrying out nitroso reduction reaction on the compound 8 to obtain the Na molecular fluorescent intermediate. The method is beneficial to improving the yield of the Na molecular fluorescentintermediate.

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