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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 75896-68-3 Chemical Structure| 75896-68-3

Structure of 75896-68-3

Chemical Structure| 75896-68-3

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Product Details of [ 75896-68-3 ]

CAS No. :75896-68-3
Formula : C11H10ClNO
M.W : 207.66
SMILES Code : COC1=CC=C2C(Cl)=CC(C)=NC2=C1
MDL No. :MFCD09787735

Safety of [ 75896-68-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H318
Precautionary Statements:P280-P301+P310-P305+P351+P338
Class:8(6.1)
UN#:2923
Packing Group:

Application In Synthesis of [ 75896-68-3 ]

* 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 [ 75896-68-3 ]

[ 75896-68-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75896-68-3 ]
  • [ 157837-31-5 ]
  • 7-methoxy-2-methyl-N-[3-(oxazol-5-yl)phenyl]quinolin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
95.17% With indium(III) chloride; In acetonitrile; at 110 - 170℃;Microwave irradiation; General procedure: To a solution of 3-aminobiphenyl derivatives with appropriate substituted group of 4-chloroquinoline in 10-15mL acetonitrile, and added indium (III) chloride as the catalyst in the Glass vial, followed by placing in the microwave reactor. Microwave wattage was between 300 and 900W, heating at 110C to 170C for 30min to 3h. After the completion of reaction, the mixture was concentrated under vacuum and then subjected to purify by flash chromatography with different proportion of dichloromethane/methanol. The solid was recrystallized in acetonitrile and filtered to obtained the desired compound.
95.17% With indium(III) chloride; In acetonitrile; at 110 - 170℃;Microwave irradiation; General procedure: To a solution of 3-aminobiphenyl derivatives with appropriate substituted group of 4-chloroquinoline in 10-15mL acetonitrile, and added indium (III) chloride as the catalyst in the Glass vial, followed by placing in the microwave reactor. Microwave wattage was between 300 and 900W, heating at 110C to 170C for 30min to 3h. After the completion of reaction, the mixture was concentrated under vacuum and then subjected to purify by flash chromatography with different proportion of dichloromethane/methanol. The solid was recrystallized in acetonitrile and filtered to obtained the desired compound.
 

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