1291090-23-7

Basic information

• Product Name: N-[4-(2-amino-9H-purin-6-yloxymethyl)-benzyl]-2-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetamide
• Synonyms: N-[4-(2-amino-9H-purin-6-yloxymethyl)-benzyl]-2-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetamide
• CAS NO: 1291090-23-7
• Molecular Weight: 642.717
• Mol File: 1291090-23-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[4-(2-amino-9H-purin-6-yloxymethyl)-benzyl]-2-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(2-amino-9H-purin-6-yloxymethyl)-benzyl]-2-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetamide(1291090-23-7)
• EPA Substance Registry System: N-[4-(2-amino-9H-purin-6-yloxymethyl)-benzyl]-2-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetamide(1291090-23-7)

Safety Data

• Hazardous Substances Data: 1291090-23-7(Hazardous Substances Data)

Upstream product

• 10310-21-1 2-amino-6-chloropurine 
• 171723-95-8 2,2,2-trifluoro-N-[[4-(hydroxymethyl)phenyl]methyl]acetamide 
• 39895-56-2 4-hydroxymethyl-benzylamine 
• 1129-35-7 4-cyanobenzoic acid methyl ester 
• 34798-95-3 2-amino-trimethylpurin-6-ylammonium chloride 
• 1291090-36-2 [8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetic acid 
• 1291090-32-8 [8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-acetic acid tert-butyl ester 
• 680622-70-2 N-[4-(2-amino-9H-purin-6-yloxymethyl)benzyl]-2,2,2-trifluoroacetamide 
• 1125471-66-0 8-[4-(dimethylamino)phenyl]-1,2-dimethylpyrano[3,2-e]indol-7(3H)-one 

Relevant articles and documents

Syntheses and characterizations of novel pyrrolocoumarin probes for SNAP-tag labeling technology

SNAP-tag technology is a revolutionary protein labeling technology employing in various biological studies. Since low signal/noise ratio and severe overlap between the FRET donors/acceptors often occurred in applying present fluorescent probes and thus limited the further applications, development of new fluorescent probes with excellent fluorescent properties is still of request by today's SNAP-tag technology. In this paper, a number of SNAP-tag protein probes have been developed by incorporating a novel pyrrolocoumarin fluorophore recently developed by our group. Examination of these novel synthetic compounds shows all these materials possess satisfactory fluorescent properties. Among these, probe 7 exhibits the most excellent characters, and its quantum yield, maximum emission wavelength and Stocks shift reach to 0.44, 534 nm and 112 nm, respectively. Further analysis of structure-property relationship indicates that the probes with a longer C3-substituted alkyl (such as pentyl) give stronger fluorescence.