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Chemical Structure| 1486-47-1 Chemical Structure| 1486-47-1

Structure of 1486-47-1

Chemical Structure| 1486-47-1

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Product Details of [ 1486-47-1 ]

CAS No. :1486-47-1
Formula : C28H23ClO4
M.W : 458.93
SMILES Code : O=C(Cl)C1=CC(OCC2=CC=CC=C2)=C(OCC3=CC=CC=C3)C(OCC4=CC=CC=C4)=C1

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Application In Synthesis of [ 1486-47-1 ]

* 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 [ 1486-47-1 ]

[ 1486-47-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 70424-94-1 ]
  • [ 1486-47-1 ]
YieldReaction ConditionsOperation in experiment
[00102] Scheme 1. Synthesis of the benzyloxybenzoyl chlorides 5 [00103] In terms of the core aromatic ring, pyrogallol 8 (present in 2a) and 3- methoxycatechol 6a (X = OMe, Y = H, present in la) were chosen. Two halogen substituted phenols, 6b (X = H, Y = CI) and 6c (X = F, Y = H) were chosen to provide a p-donor (similar to the methoxy group) but electron withdrawing group. An unsubstituted catechol 6d (X, Y = H) was included. As shown in Scheme 2, each of these phenols was then coupled to each of the acid chlorides 5a-f and several methoxy-substituted benzoyl chlorides. After coupling, the benzyloxy esters were deprotected via catalytic hydrogenation. The overall yields are shown in Table 2.
  • 2
  • [ 1486-47-1 ]
  • [ 863-03-6 ]
  • 3
  • [ 363-52-0 ]
  • [ 1486-47-1 ]
  • C62H49FO10 [ No CAS ]
 

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