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[ CAS No. 7025-33-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 7025-33-4
Chemical Structure| 7025-33-4
Structure of 7025-33-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 7025-33-4 ]

CAS No. :7025-33-4 MDL No. :MFCD00268737
Formula : C15H9BrN2S Boiling Point : -
Linear Structure Formula :- InChI Key :KEPQCZGPWRNPCZ-UHFFFAOYSA-N
M.W : 329.21 Pubchem ID :667715
Synonyms :

Safety of [ 7025-33-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330 UN#:N/A
Hazard Statements:H302-H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 7025-33-4 ]

* 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 [ 7025-33-4 ]

[ 7025-33-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7025-33-4 ]
  • [ 1160294-96-1 ]
  • C51H34N4S [ No CAS ]
YieldReaction ConditionsOperation in experiment
1.65 g With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate In toluene at 100℃; for 24h; 6 Synthesis Example 6: Synthesis of compound B2 To a 100 mL round bottom flask was added S2 (2.00 g, 4.11 mmol), G4 (1.37 g, 4.14 mmol) Tris (dibenzylideneacetone) dipalladium (0) (0.06 g, 0.06 mmol),Tri-tert-butylphosphine (0.02 g, 0.12 mmol) and sodium tert-butoxide (0.55 g, 5.75 mmol)After dissolving in toluene (40 mL), the mixture was stirred in a bath at 100 ° C for 24 hours. After completion of the reaction, toluene was removed, and the residue was extracted with dichloromethane and water.The column was separated by using ethyl acetate and n-hexane. Then, the precipitate was prepared by using dichloromethane and petroleum ether,Filtration gave Compound B2 (1.65 g, 2.13 mmol). NMR analysis results of the synthesized B2 compound are shown in Fig.
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