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[ CAS No. 16927-84-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 16927-84-7
Chemical Structure| 16927-84-7
Structure of 16927-84-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 16927-84-7 ]

CAS No. :16927-84-7 MDL No. :MFCD15209649
Formula : C14H14O Boiling Point : -
Linear Structure Formula :- InChI Key :ZCJANMPFIVCFCY-UHFFFAOYSA-N
M.W : 198.26 Pubchem ID :264324
Synonyms :

Safety of [ 16927-84-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 16927-84-7 ]

* 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 [ 16927-84-7 ]

[ 16927-84-7 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 16927-84-7 ]
  • [ 1812-51-7 ]
YieldReaction ConditionsOperation in experiment
With copper chromite at 200℃; Hydrogenolyse;
  • 4
  • [ 16927-84-7 ]
  • [ 1812-51-7 ]
YieldReaction ConditionsOperation in experiment
at 200℃;
  • 5
  • [ 7664-93-9 ]
  • [ 16927-84-7 ]
  • [ 64-19-7 ]
  • K2cr2O7 [ No CAS ]
  • [ 2142-66-7 ]
  • 6
  • [ 265671-40-7 ]
  • [ 5411-56-3 ]
  • [ 16927-84-7 ]
  • 7
  • [ 108-22-5 ]
  • [ 2142-66-7 ]
  • (R)-1-(biphenyl-2-yl)ethyl acetate [ No CAS ]
  • [ 16927-84-7 ]
  • 9
  • [ 5411-56-3 ]
  • [ 98-80-6 ]
  • [ 16927-84-7 ]
YieldReaction ConditionsOperation in experiment
80% With C32H26NO2PPdS; potassium carbonate; In ethanol; N,N-dimethyl acetamide; water; at 100℃; for 12h;Catalytic behavior; General procedure: To the catalyst (1.0 mol%) dissolved in 1 ml DMAc, aryl bromide (1.0 mmol), phenyl boronic acid (1.5 mmol) in 1 ml ethanol, K2CO3 (2.0 mmol) in 1 ml water and DMAc (5 ml) were all added. The mixture was heated at 100 C for 12 h. Then, the mixture was cooled, water was added and the product was extracted with ethylacetate. The organic layer was washed with brine, dried over Na2SO4, filtered, passed through celite, and analyzed by GC. Yields were based on corresponding aryl bromides.
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