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Chemical Structure| 20035-42-1 Chemical Structure| 20035-42-1

Structure of 20035-42-1

Chemical Structure| 20035-42-1

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Product Details of [ 20035-42-1 ]

CAS No. :20035-42-1
Formula : C8H6Br2O3
M.W : 309.94
SMILES Code : O=CC1=C(O)C(OC)=CC(Br)=C1Br
MDL No. :MFCD00046151

Safety of [ 20035-42-1 ]

Application In Synthesis of [ 20035-42-1 ]

* 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 [ 20035-42-1 ]

[ 20035-42-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1123-93-9 ]
  • [ 20035-42-1 ]
  • (E)-2-((benzo[d]thiazol-5-ylimino)methyl)-3,4-dibromo-6-methoxyphenol [ No CAS ]
YieldReaction ConditionsOperation in experiment
87.5% With acetic acid; In i-Amyl alcohol;Reflux; Inert atmosphere; 2,3-Dibromo-6-hydroxy-5-methoxybenzaldehyde (0.1 g, 0.32 mmol), 5-benzothiazolamine (0.03 g, 0.21 mmol), and isoamyl alcohol (2 mL) were stirred at room temperature under N2. Acetic acid (0.07 mL) was added drop-wise, and the mixture was refluxed overnight. The reaction mixture was filtered, washed with CH2Cl2, MeOH, and dried to yield 27 (0.08 g, 0.18 mmol, 87.5percent) as an orange powder. 1H NMR (DMSO, 300 MHz) delta 15.12 (s, 1H), 9.49 (s, 1H), 9.25 (s, 1H), 8.29 (d, 1H, J=8.4 Hz), 8.22 (d, 1H, J=1.8 Hz), 7.65 (dd, 1H, J=8.4 Hz, 1.8 Hz), 7.42(s, 1H), 3.86 (s, 3H); 13C NMR (DMSO, 700 MHz) delta 164.89, 158.70, 154.49, 154.33, 149.34, 145.16, 133.37, 124.00, 121.49, 120.28, 119.30, 117.71, 115.64, 113.35, 57.07. Rf=0.59 (Hexane/EtOAc 2:1)
87.5% With acetic acid; In i-Amyl alcohol;Inert atmosphere; Reflux; 2,3-dibromo-6-hydroxy-5-methoxybenzaldehyde (0.1g, 0.32 mmol), 5- benzothiazolyl asleep Min (0.03g, 0.21 mmol) and isoamyl alcohol (2 mL) and N2It was stirred at room temperature.It was added dropwise acetic acid (0.07 mL) and the mixture was refluxed overnight.Filtering the reaction mixture, CH2Cl2and dried and then washed with MeOH, the orange powder obtained in27to give a (0.08g, 0.18mmol, 87.5percent).
 

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• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Dihalides • Reactions of Ethers • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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