1033736-87-6

Basic information

• Product Name: C₁₆H₁₀O₃S
• Synonyms: C₁₆H₁₀O₃S
• CAS NO: 1033736-87-6
• Molecular Weight: 282.32
• Mol File: 1033736-87-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₀O₃S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₀O₃S(1033736-87-6)
• EPA Substance Registry System: C₁₆H₁₀O₃S(1033736-87-6)

Safety Data

• Hazardous Substances Data: 1033736-87-6(Hazardous Substances Data)

Upstream product

• 1187758-97-9 (1,1-dioxido-4-oxo-3-phenyl-4H-thiochromen-2-yl)methyl diethyl phosphate 
• 1033736-99-0 (4-oxo-3-phenyl-4H-1,1-dioxothiochromen-2-yl)methyl dodecanoate 
• 1033736-90-1 C₃₈H₃₀O₁₀S₂ 
• 1033736-93-4 4-hydroxybutyl (4-oxo-3-phenyl-4H-thiochromen-2-yl)methylcarbonate 
• 1033736-80-9 C₃₃H₂₇NO₇S 
• 112-16-3 n-dodecanoyl chloride 
• 1033736-38-7 2-(hydroxymethyl)-3-phenyl-4H-thiochromen-4-one 1,1-dioxide 

Relevant articles and documents

Study of the Paternò–Büchi type photolabile protecting group and application to various acids

An efficient photolabile protecting group, thiochromone S,S-dioxides with the diazomethyl group for phosphate derivatives, amino acids and sulfonic acids was developed. Protection and photodeprotection reactions proceeded smoothly under mild conditions without any catalyst.1H NMR and HPLC spectra studies demonstrated the photolysis properties of the photolabile protecting group and gave an exact quantification of the released substrates. Specially, the photoproduct derived from the thiochromone derivatives following Paternò–Büchi type photo-cycloaddition showed high fluorescence intensity. This fluorescent characteristic demonstrated the photodeprotection progress also can be monitored by fluorescence spectra.