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Chemical Structure| 1218-89-9 Chemical Structure| 1218-89-9

Structure of 1218-89-9

Chemical Structure| 1218-89-9

2-Hydroxy-1,2-di-p-tolylethanone

CAS No.: 1218-89-9

4.5 *For Research Use Only !

Cat. No.: A237448 Purity: 98%

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Product Details of [ 1218-89-9 ]

CAS No. :1218-89-9
Formula : C16H16O2
M.W : 240.30
SMILES Code : OC(C1=CC=C(C)C=C1)C(C2=CC=C(C)C=C2)=O
MDL No. :MFCD00008555
Boiling Point : No data available
InChI Key :NBYSFWKNMLCZLO-UHFFFAOYSA-N
Pubchem ID :224848

Safety of [ 1218-89-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1218-89-9 ]

* 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 [ 1218-89-9 ]

[ 1218-89-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 50-00-0 ]
  • [ 1218-89-9 ]
  • [ 4079-54-3 ]
  • (S)-2-hydroxy-1,2-bis(4-methylphenyl)ethan-1-one [ No CAS ]
  • 2
  • [ 1218-89-9 ]
  • [ 137-07-5 ]
  • [ 16112-21-3 ]
YieldReaction ConditionsOperation in experiment
85.7% With silica gel-supported chlorosulfonic acid; In 2-methyltetrahydrofuran; at 120℃; for 4h; At room temperature, to the reaction vessel in an organic solvent, 2-MeTHF was added the above formula (II) Compound of formula (III) compound and silica-supported chlorosulfonic acid. Wherein, the formula (II) and the formula (III) The molar ratio of the compound of 1: 2 molar ratio of formula (II) compound with chlorosulfonic acid is 1: 0.1; stir Mix warmed up to 120 C, and incubated for 4 hours.After post-processing, as a yellow crystalline product of the formula (the I), in a yield of 85.7%, Purity 98.4% (HPLC).
 

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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 of Benzene and Substituted Benzenes • 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

Categories

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