910095-75-9

Basic information

• Product Name: C₆₉H₉₆N₄O₁₈S₂
• Synonyms: C₆₉H₉₆N₄O₁₈S₂
• CAS NO: 910095-75-9
• Molecular Weight: 1333.67
• Mol File: 910095-75-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₆₉H₉₆N₄O₁₈S₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₉H₉₆N₄O₁₈S₂(910095-75-9)
• EPA Substance Registry System: C₆₉H₉₆N₄O₁₈S₂(910095-75-9)

Safety Data

• Hazardous Substances Data: 910095-75-9(Hazardous Substances Data)

Upstream product

• 910055-76-4 carbonic acid 3-tert-butoxycarbonylamino-6-({tert-butoxycarbonyl-[4-(3-hydroxy-phenoxy)-butyl]-amino}-methyl)-4,5-dihydroxy-tetrahydro-pyran-2-yl ester tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 102-29-4 Resorcinol monoacetate 
• 14257-69-3 glucosamine 
• 910055-74-2 Acetic acid 3-{4-[((2R,3S,4R,5R,6S)-5-tert-butoxycarbonylamino-6-tert-butoxycarbonyloxy-3,4-dihydroxy-tetrahydro-pyran-2-ylmethyl)-amino]-butoxy}-phenyl ester 
• 910055-68-4 Toluene-4-sulfonic acid (2R,3S,4R,5R,6S)-5-tert-butoxycarbonylamino-6-tert-butoxycarbonyloxy-3,4-dihydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 910055-70-8 6-amino-6-deoxy-1-O-(tert-butoxycarbonyl)-2-N-(tert-butoxycarbonyl)-β-D-glucosamine 
• 910055-69-5 6-azido-6-deoxy-1-O-(tert-butoxycarbonyl)-2-N-(tert-butoxycarbonyl)-β-D-glucosamine 
• 862291-55-2 1-O-(tert-butoxycarbonyl)-2-N-(tert-butoxycarbonyl)-β-D-glucosamine 
• 178158-23-1 N-Cbz-D-glucosamine 
• 910055-73-1 3-(4-iodobutoxy)phenyl acetate 
• 910055-75-3 acetic acid 3-{4-[tert-butoxycarbonyl-(5-tert-butoxycarbonylamino-6-tert-butoxycarbonyloxy-3,4-dihydroxy-tetrahydro-pyran-2-ylmethyl)-amino]-butoxy}-phenyl ester 

Relevant articles and documents

Synthesis and characterization of glucosamine-bound near-infrared probes for optical imaging

Two novel near-infrared (NIR) fluorescent probes have been synthesized by linking a carbocyanine fluorophore and glucosamine through different linkers. These probes demonstrated a high quantum yield, low cytotoxicity, reversible pH-dependent fluorescence in the physiological pH range, and a decreased aggregation tendency in aqueous solutions. In vitro NIR optical imaging studies revealed cellular uptake and strong intracellular NIR fluorescence of these two probes in four breast epithelial cell lines.