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[ CAS No. 1309982-38-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1309982-38-4
Chemical Structure| 1309982-38-4
Structure of 1309982-38-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1309982-38-4 ]

CAS No. :1309982-38-4 MDL No. :MFCD09839169
Formula : C16H24BNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :LJTZQZOLQCVMCV-UHFFFAOYSA-N
M.W : 305.18 Pubchem ID :53398532
Synonyms :

Safety of [ 1309982-38-4 ]

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

Application In Synthesis of [ 1309982-38-4 ]

* 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 [ 1309982-38-4 ]

[ 1309982-38-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 263270-02-6 ]
  • [ 73183-34-3 ]
  • [ 1309982-38-4 ]
YieldReaction ConditionsOperation in experiment
With 1,1'-bis-(diphenylphosphino)ferrocene; potassium acetate In 1,4-dioxane at 100℃; 2-6 Reference Example 2-6:[S-ftert-ButoxycarbonvDpyridin-S-yliboronic acidPd(OAc)2 (0.112 g, 0.500 mmol), DPPF (0.554 g, 1.000 mmol), KOAc (1.18 g, 12.0 mmol), tert-butyl 5-bromonicotinate (2.58 g, 10.0 mmol) and bis(pinacolato)diboran (2.79 g, 11.0 mmol) were suspended in 1,4-dioχane (25 ml) and the mixture was stirred at 100°C overnight. The mixture was filtered through celite pad, and the filtrate was evaporated in vacuo. The residue was suspended in acetone (25.0 ml) / H2O (25.0 ml), and sodium periodate (6.41 g,30.0 mmol) and ammonium acetate (2.31 g, 30.0 mmol) were added thereto. The mixture wε. stirred at room temperature for overnight and was diluted with CHCI3 and H2O. The organic layer was washed with H2O, brine, and dried over MgSOφ After flteration and evaporation, the residue was purified by silicagel colunm chromatography (CHCI3 / MeOH) to give intended compound as a brown solid.
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