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Chemical Structure| 103796-41-4 Chemical Structure| 103796-41-4
Chemical Structure| 103796-41-4

1,2,3,4-Tetrahydroquinolin-6-amine

CAS No.: 103796-41-4

4.5 *For Research Use Only !

Cat. No.: A441342 Purity: 95+%

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Product Details of [ 103796-41-4 ]

CAS No. :103796-41-4
Formula : C9H12N2
M.W : 148.21
SMILES Code : NC1=CC2=C(NCCC2)C=C1
MDL No. :MFCD09260888

Safety of [ 103796-41-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
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

Application In Synthesis of [ 103796-41-4 ]

* 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 [ 103796-41-4 ]

[ 103796-41-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 580-15-4 ]
  • [ 103796-41-4 ]
YieldReaction ConditionsOperation in experiment
With hydrogen; In methanol; at 80℃; under 30003.0 Torr; for 24h;Autoclave; General procedure: In a typical reaction, 30 mg of catalyst was added into the Tefloninner container. Then, 1 mmol of quinoline (0.129 g) was carefullyadded dropwise to the container, which was transferred into a 16 mL ofstainless steel autoclave. To remove the air, 1 MPa of H2 was charged tothe sealed autoclave for three times. Then, 4 MPa of H2 was charged tothe reactor, which was heated to 50 C. Upon the reaction completion,the autoclave was naturally cooled to room temperature, and then thegas in the reactor slowly emitted. The liquid products were analyzed ona gas chromatograph (GC-9720, Fuli) and GC-MS (6890N-5975,Agilent).
 

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