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[ CAS No. 6093-68-1 ] {[proInfo.proName]}

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Chemical Structure| 6093-68-1
Chemical Structure| 6093-68-1
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Product Details of [ 6093-68-1 ]

CAS No. :6093-68-1 MDL No. :MFCD00630040
Formula : C9H6O3 Boiling Point : -
Linear Structure Formula :- InChI Key :CJIJXIFQYOPWTF-UHFFFAOYSA-N
M.W : 162.14 Pubchem ID :99477
Synonyms :
Chemical Name :6-Hydroxy-2H-chromen-2-one

Safety of [ 6093-68-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 6093-68-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 6093-68-1 ]

[ 6093-68-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6093-68-1 ]
  • [ 6608-47-5 ]
  • 2-oxo-2H-chromen-6-yl ethenesulfonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% With triethylamine; In tetrahydrofuran; at 20℃; for 4h; General procedure: Coumarin sulfonates derivatives 4-43 were synthesized byreacting 3-hydroxy coumarin 1, 4-hydroxy coumarin 2 and 6-hydroxy coumarin 3 derivatives (1 mmol) with commercially available sulfonyl chlorides derivatives (1.2 mmol) in THF(15 mL) in the presence of triethyl amine (1 mmol). Reaction mixture was stirred for 4 h at room temperature to afford coumarin sulfonates 4-43. TLC monitoring was used to determine the progressof the reaction. After the completion of reaction, THF was evaporated and then solid product was washed with distilled water and dried under vacuum. The products were crystallized from methanol afforded good yields (Scheme 1).
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Technical Information

? Acyl Group Substitution ? Appel Reaction ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Bouveault-Blanc Reduction ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Catalytic Hydrogenation ? Chugaev Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Ester Cleavage ? Fischer Indole Synthesis ? Grignard Reaction ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Jones Oxidation ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Martin's Sulfurane Dehydrating Reagent ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mitsunobu Reaction ? Moffatt Oxidation ? Oxidation of Alcohols by DMSO ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Amines ? Prins Reaction ? Reactions of Alcohols ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Ritter Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Stobbe Condensation ? Swern Oxidation ? Tebbe Olefination ? Ugi Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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