1345614-77-8

Basic information

• Product Name: acetic acid 4-(1{3-[7-(tert-butyldimethylsilanyloxy)-3,4-dihydro-2H-quinolin-1-yl]propane-1-sulfonyloxy}-2,2,2-trifluoroethyl)phenyl ester
• Synonyms: acetic acid 4-(1{3-[7-(tert-butyldimethylsilanyloxy)-3,4-dihydro-2H-quinolin-1-yl]propane-1-sulfonyloxy}-2,2,2-trifluoroethyl)phenyl ester
• CAS NO: 1345614-77-8
• Molecular Weight: 601.76
• Mol File: 1345614-77-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: acetic acid 4-(1{3-[7-(tert-butyldimethylsilanyloxy)-3,4-dihydro-2H-quinolin-1-yl]propane-1-sulfonyloxy}-2,2,2-trifluoroethyl)phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: acetic acid 4-(1{3-[7-(tert-butyldimethylsilanyloxy)-3,4-dihydro-2H-quinolin-1-yl]propane-1-sulfonyloxy}-2,2,2-trifluoroethyl)phenyl ester(1345614-77-8)
• EPA Substance Registry System: acetic acid 4-(1{3-[7-(tert-butyldimethylsilanyloxy)-3,4-dihydro-2H-quinolin-1-yl]propane-1-sulfonyloxy}-2,2,2-trifluoroethyl)phenyl ester(1345614-77-8)

Safety Data

• Hazardous Substances Data: 1345614-77-8(Hazardous Substances Data)

Upstream product

• 22246-18-0 7-hydroxy-3,4-dihydro-2-(1H)-quinolinone 
• 1233524-42-9 7-(tert-butyldimethylsilanyloxy)-1,2,3,4-tetrahydroquinoline 
• 1345614-63-2 acetic acid 4-[1-(3-iodopropane-1-sulfonyloxy)-2,2,2-trifluoroethyl]phenyl ester 
• 1345614-61-0 acetic acid 4-[1-(3-chloropropane-1-sulfonyloxy)-2,2,2-trifluoroethyl]phenyl ester 
• 58196-33-1 7-hydroxy-1,2,3,4-tetrahydroquinoline 
• 1279691-41-6 acetic acid 4-(2,2,2-trifluoro-1-hydroxyethyl)phenyl ester 

Downstream Products

• 1345614-80-3 1,11-bis{3-[1-(4-acetoxyphenyl)-2,2,2-trifluoroethoxysulfonyl]propyl}-3,4,8,9,10,11-hexahydro-2H-13-oxa-6,11-diaza-1-azonia-pentacene tetrafluoroborate 

Relevant articles and documents

Synthesis of near-IR fluorescent oxazine dyes with esterase-labile sulfonate esters

Near-IR oxazine dyes are reported that contain sulfonate esters which are rapidly cleaved by esterase activity to unmask highly polar anionic sulfonates. Strategies for the synthesis of these dyes included the development of milder dye condensation conditions with improved functional compatibility and the use of an alkyl halide that allows for the introduction of esterase-labile sulfonates without the need for sulfonation of the target molecule.