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[ CAS No. 63660-21-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 63660-21-9
Chemical Structure| 63660-21-9
Structure of 63660-21-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 63660-21-9 ]

CAS No. :63660-21-9 MDL No. :N/A
Formula : C30H29BrN2O7 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 609.46 Pubchem ID :-
Synonyms :

Safety of [ 63660-21-9 ]

Signal Word: Class:N/A
Precautionary Statements: UN#:N/A
Hazard Statements: Packing Group:N/A

Application In Synthesis of [ 63660-21-9 ]

* 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 [ 63660-21-9 ]

[ 63660-21-9 ] Synthesis Path-Downstream   1~2

  • 2
  • bis(4-methoxyphenyl)phenylmethylium tetrafluoroborate [ No CAS ]
  • [ 59-14-3 ]
  • [ 63660-21-9 ]
YieldReaction ConditionsOperation in experiment
88% With lithium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20℃;Heating; The unprotected nucleoside (1 eq.) and Li2CO3 (5 eq.) were dried together overnight under vacuum (<0.1 mm Hg). A solution of N,N-diisopropylethylamine (3 eq.) in THF was then added and heated to dissolve the starting materials. The solution was cooled to room temperature and dimethoxytrityl tetrafluoroborate 10 was added in portions of 0.2-0.3 eq., in 30 min intervals. When TLC analysis indicated complete consumption of starting material, or competing formation of di-DMT-protected nucleosides was observed, the additions were stopped and the reaction was allowed to proceed for another 2 h. The mixture was then diluted with CH2Cl2, washed with sat. NaHCO3, H2O and brine, dried over MgSO4, and filtered. Solvents were removed in vacuo and the residue was purified by automated column chromatography on silica gel. Drying under vacuum (<0.1 mm Hg) afforded the DMT-protected products. A detailed representative procedure is given for the preparation of compound 4.
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