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3-Fluorostyrene | CAS:350-51-6
3-Fluorostyrene
  • Name:3-Fluorostyrene
  • CAS:350-51-6
  • Synonyms:
  • Molecular Formula:C8H7F
  • Molecular Weight:122.14
  • EINESC:206-504-9

Description

Properties

Boiling point 30-31 ºC (4 mmHg)
Flash point 29 ºC
Density 1.025
Refractive index 1.516-1.518

Safety

Symbol(GHS) Xi
Hazard Codes R10;R36/37/38
SDS/MSDS S16;S26;S37/39

SDS

Source SDS/MSDS Samples
没有数据没有数据
Synthetic Route
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Articles
Peer-Reviewed Papers
Efficient degradation of chloroquine drug by electro-Fenton oxidation: Effects of operating conditions and degradation mechanism.Sondos Midassi et al.Chemosphere, 260, 127558-127558 (2020-07-22) Synthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline.Manolo Casagrande et al.Bioorganic & medicinal chemistry, 20(19), 5965-5979 (2012-08-25) An ELISA test for detecting chloroquine in urine.F C Shenton et al.Transactions of the Royal Society of Tropical Medicine and Hygiene, 82(2), 216-220 (1988-01-01) Synthesis and comparison of antiplasmodial activity of (+), (-) and racemic 7-chloro-4-(N-lupinyl)aminoquinoline.Chiara Rusconi et al.Bioorganic & medicinal chemistry, 20(19), 5980-5985 (2012-08-21) Chloroquine metabolism in man: urinary excretion of 7-chloro-4-hydroxyquinoline and 7-chloro-4-aminoquinoline metabolites.N D Brown et al.Journal of chromatography, 345(1), 209-214 (1985-11-29) Overcoming drug resistance to heme-targeted antimalarials by systematic side chain variation of 7-chloro-4-aminoquinolines.Kimberly Yearick et al.Journal of medicinal chemistry, 51(7), 1995-1998 (2008-03-19) New chimeric antimalarials with 4-aminoquinoline moiety linked to a tetraoxane skeleton.Igor Opsenica et al.Journal of medicinal chemistry, 51(19), 6216-6219 (2008-09-09) Synthesis and antimalarial activity study of some new Mannich bases of 7-chloro-4-aminoquinoline.Susanta Roy et al.Medicinal chemistry (Shariqah (United Arab Emirates)), 9(3), 379-383 (2012-09-06) Synthesis, antimalarial activity, and cellular toxicity of new arylpyrrolylaminoquinolines.Manolo Casagrande et al.Bioorganic & medicinal chemistry, 18(18), 6625-6633 (2010-08-28)
Remarks

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