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Chemical Structure| 17150-62-8 Chemical Structure| 17150-62-8

Structure of N-Benzylbut-3-en-1-amine
CAS No.: 17150-62-8

Chemical Structure| 17150-62-8

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Product Details of [ 17150-62-8 ]

CAS No. :17150-62-8
Formula : C11H15N
M.W : 161.24
SMILES Code : C=CCCNCC1=CC=CC=C1
MDL No. :MFCD01249643
InChI Key :DGTNEDHBSGFIBX-UHFFFAOYSA-N
Pubchem ID :4366091

Safety of [ 17150-62-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 17150-62-8 ]

* 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 [ 17150-62-8 ]

[ 17150-62-8 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 17150-62-8 ]
  • [ 1204-06-4 ]
  • (E)-N-benzyl-N-(but-3-en-1-yl)-3-(1H-indol-3-yl)acrylamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
67% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20℃;Inert atmosphere; General procedure: Homoallylbenzylamine 7 (1.0 mmol) was added to a mixture of the corresponding carboxylic acid 5 (1.0 mmol), EDCI (1.5 mmol), HOBt (2.0 mmol) and triethylamine (2.0 mmol) in DCM (0.10 M). The mixture was stirred overnight at rt. The reaction mixture was then hydrolysed with H2O (20 mL) and extracted with DCM (3 × 15 mL). Collected organic fractions were dried over Na2SO4 and, after removal of the solvents the crude reaction mixture was purified by flash chromatography.
  • 3
  • [ 1181816-12-5 ]
  • [ 17150-62-8 ]
  • C22H32N2O2 [ No CAS ]
 

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