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Chemical Structure| 3658-77-3 Chemical Structure| 3658-77-3
Chemical Structure| 3658-77-3

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4-Hydroxy-2,5-dimethyl-3(2H)furanone is a naturally occurring substance found in a variety of fruits and has been shown to have antimicrobial activity.

Synonyms: 4-Hydroxy-2,5-dimethyl-3(2H)furanone; HDMF

4.5 *For Research Use Only !

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Product Details of Furaneol

CAS No. :3658-77-3
Formula : C6H8O3
M.W : 128.13
SMILES Code : O=C1C(C)OC(C)=C1O
Synonyms :
4-Hydroxy-2,5-dimethyl-3(2H)furanone; HDMF
MDL No. :MFCD00010706
InChI Key :INAXVXBDKKUCGI-UHFFFAOYSA-N
Pubchem ID :19309

Safety of Furaneol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of Furaneol

* 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.

  • Upstream synthesis route of [ 3658-77-3 ]

[ 3658-77-3 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 87-72-9 ]
  • [ 56-41-7 ]
  • [ 3658-77-3 ]
  • [ 27538-10-9 ]
References: [1] Journal of Agricultural and Food Chemistry, 1996, vol. 44, # 2, p. 531 - 536.
  • 2
  • [ 58-86-6 ]
  • [ 56-41-7 ]
  • [ 3658-77-3 ]
  • [ 27538-10-9 ]
References: [1] Journal of Agricultural and Food Chemistry, 2003, vol. 51, # 9, p. 2708 - 2713.
  • 3
  • [ 58-86-6 ]
  • [ 56-40-6 ]
  • [ 3658-77-3 ]
  • [ 27538-10-9 ]
References: [1] Journal of Agricultural and Food Chemistry, 2003, vol. 51, # 9, p. 2708 - 2713.
 

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Technical Information

• Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • 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-Ketenes • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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