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Chemical Structure| 705-15-7 Chemical Structure| 705-15-7
Chemical Structure| 705-15-7

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Synonyms: 2-Hydroxy-5-methoxyacetophenone

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Product Citations

Product Citations

Han, Guanqun ;

Abstract: Mankind's sustainable development not only requires the capture and conversion of renewable energies but also necessitates the production of chemical goods from renewable carbon sources. Biomass is the only accessible and renewable carbon source. One major class of biomass is degradative small molecules, among which 5-hydroxymethylfurfural (HMF) is considered as a platform chemical and it can serve as a starting material to produce various upgrading compounds, eg, the oxidation products, 2, 5-furan dicarboxylic acid (FDCA), and 2, 5-diformylfuran (DFF), can act as biopolymer precursors. In this dissertation, we successfully demonstrated that ultrathin Ni/CdS nanosheets can be efficient photocatalyst to produce value-added bioproducts (eg, furoic acid, DFF, and FDCA) from biomass-derived molecules. Even more desirable is that the oxidative biomass upgrading can be integrated with H2 production.

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Product Details of 2′-Hydroxy-5′-methoxyacetophenone

CAS No. :705-15-7
Formula : C9H10O3
M.W : 166.17
SMILES Code : CC(C1=CC(OC)=CC=C1O)=O
Synonyms :
2-Hydroxy-5-methoxyacetophenone
MDL No. :MFCD00008731
InChI Key :MLIBGOFSXXWRIY-UHFFFAOYSA-N
Pubchem ID :69714

Safety of 2′-Hydroxy-5′-methoxyacetophenone

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2′-Hydroxy-5′-methoxyacetophenone

* 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 [ 705-15-7 ]
  • Downstream synthetic route of [ 705-15-7 ]

[ 705-15-7 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 108-86-1 ]
  • [ 705-15-7 ]
  • [ 201230-82-2 ]
  • [ 26964-24-9 ]
References: [1] Chemistry - A European Journal, 2012, vol. 18, # 40, p. 12595 - 12598.
  • 2
  • [ 705-15-7 ]
  • [ 26964-24-9 ]
References: [1] Journal of the Chinese Chemical Society, 2004, vol. 51, # 6, p. 1389 - 1394.
[2] Journal of Organic Chemistry, 1991, vol. 56, # 26, p. 7292 - 7297.
[3] Advanced Synthesis and Catalysis, 2018, vol. 360, # 6, p. 1218 - 1231.
[4] Molecules, 2018, vol. 23, # 9, .
  • 3
  • [ 705-15-7 ]
  • [ 100-52-7 ]
  • [ 26964-24-9 ]
References: [1] Organic and Biomolecular Chemistry, 2011, vol. 9, # 20, p. 6930 - 6933.
 

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Technical Information

• Acidity of Phenols • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Chan-Lam Coupling Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Electrophilic Substitution of the Phenol Aromatic Ring • Etherification Reaction of Phenolic Hydroxyl Group • Fischer Indole Synthesis • Friedel-Crafts Reaction • Grignard Reaction • Halogenation of Phenols • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Nomenclature of Ethers • Oxidation of Phenols • Passerini Reaction • Paternò-Büchi Reaction • Pechmann Coumarin Synthesis • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Preparation of Ethers • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • Reformatsky Reaction • Reimer-Tiemann Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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