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[ CAS No. 75954-35-7 ] {[proInfo.proName]}

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Chemical Structure| 75954-35-7
Chemical Structure| 75954-35-7
Structure of 75954-35-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 75954-35-7 ]

CAS No. :75954-35-7 MDL No. :MFCD00471947
Formula : C13H11BrS Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 279.20 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 75954-35-7 ]

* 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 [ 75954-35-7 ]

[ 75954-35-7 ] Synthesis Path-Downstream   1~31

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  • Methyl 4-phenylthiobenzyl ether [ No CAS ]
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  • Methyl 4-phenylthiobenzyl ether [ No CAS ]
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  • Phenyl 4-phenylthiobenzyl ether [ No CAS ]
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  • 11
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  • Phenyl 4-phenylthiobenzyl ether [ No CAS ]
  • 12
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  • 4-bromo-benzyl halide [ No CAS ]
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  • 15
  • [ 28074-23-9 ]
  • p-brombenzylbis(dimethylglyoximato)pyridinecobalt(III) [ No CAS ]
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  • 16
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  • 21
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  • sodium 4-bromobenzylsulfanesulfonate [ No CAS ]
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  • 22
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  • 23
  • [ 882-33-7 ]
  • 4-bromobenzyl diphenylphosphinite [ No CAS ]
  • [ 75954-35-7 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 20℃; for 12h;Inert atmosphere; General procedure: To a stirred solution of alcohol (1 mmol), Et3N (1.2 equiv.) in dry CH2Cl2 (1 mL) was successively added chlorodiphenylphosphine (1.2 equiv.) at RT under N2 atmosphere. After 2 h, benzothiazole-2-thiol (0.5 equiv.) and camphorquinone (1 equiv.) were added to the mixture, respectively. After the mixture was stirred for 12 h, it was extracted with CH2Cl2/H2O. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by preparative TLC on silica gel (hexane/EtOAc = 10/1) to afford the desired product.
  • 24
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  • 26
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YieldReaction ConditionsOperation in experiment
89% With cobalt ferrite; potassium acetate; thiourea; In dimethyl sulfoxide; at 80℃; for 1.5h; A glass tube was charged with nitroarene (1 mmol), alkyl halide (1.2 mmol), thiourea (1.3 mmol), KOAc (1.5 mmol), DMSO (1 mL) and CoFe2O4 (5 mol%). The reaction mixture was stirred at 80 C for an appropriate amount of time. The progress of the reaction was monitored using TLC (n-hexane-EtOAc, 9:1). After completion of the reaction, the reaction mixture was allowed to cool to room temperature. The magnetic nanoparticles of the catalyst were collected using a magnet. Then, 10mL of water was added to the mixture and the product was extracted with ethyl acetate (3 × 10 mL). The organic phase was dried over CaCl2, concentrated under vacuum and purified by column chromatography on silica gel (n-hexane-EtOAc, 9:1). All products were known compounds and were identified by comparison of their 1H NMR spectra with those of authentic samples [25,26].
  • 27
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  • 31
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  • [ 22979-35-7 ]
  • methyl 3-(4-bromophenyl)-2-phenyl-2-(phenylthio)propanoate [ No CAS ]
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