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Chemical Structure| 544707-13-3 Chemical Structure| 544707-13-3

Structure of 544707-13-3

Chemical Structure| 544707-13-3

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Product Details of [ 544707-13-3 ]

CAS No. :544707-13-3
Formula : C11H10O2
M.W : 174.20
SMILES Code : O=CC1=CC=C(C#CCCO)C=C1
MDL No. :MFCD03406287

Safety of [ 544707-13-3 ]

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

Application In Synthesis of [ 544707-13-3 ]

* 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 [ 544707-13-3 ]

[ 544707-13-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 544707-13-3 ]
  • [ 16081-45-1 ]
  • 4-(4-((4-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)piperazin-1-yl)methyl)phenyl)but-3-yn-1-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% 1-(2,3-Dihydrobenzo[b][1,4]dioxin-5-yl)piperazine (500 mg, 2.27 mmol) and 4-(4- hydroxybut-1-yn-1-yl)benzaldehyde (475 mg, 2.27 mmol) were suspended inDMF/AcOH (50 mL/1 mL). The mixture was stirred for 30 minutes, then NaBH(OAc)3 (193 mg, 9.09 mmol) was added and the resulting reaction mixture was stirred at RT overnight. The reaction mixture was concentrated, diluted with H20 (200 ml), made alkaline with NaOH (2 M) and extracted with DCM (3 x 150 ml). The combined organic layers were dried, filtered and concentrated affording 4-(4-((4-(2,3-dihydrobenzo[b] [1 ,4]dioxin-5 -yl)piperazin- 1 -yl)methyl)phenyl)but-3 -yn- 1 -ol (0.6 g,1.59 mmol, 70%). The material obtained was used in the next step without any further purification.
 

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Technical Information

• Appel Reaction • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • 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 • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Stetter Reaction • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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