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Chemical Structure| 41532-84-7 Chemical Structure| 41532-84-7
Chemical Structure| 41532-84-7

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Product Details of 1,1,2-Trimethyl-1H-benz[e]indole

CAS No. :41532-84-7
Formula : C15H15N
M.W : 209.29
SMILES Code : CC1=NC2=C(C3=CC=CC=C3C=C2)C1(C)C
MDL No. :MFCD00082627
InChI Key :WJZSZXCWMATYFX-UHFFFAOYSA-N
Pubchem ID :170530

Safety of 1,1,2-Trimethyl-1H-benz[e]indole

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

Application In Synthesis of 1,1,2-Trimethyl-1H-benz[e]indole

* 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 [ 41532-84-7 ]

[ 41532-84-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 41532-84-7 ]
  • [ 49827-15-8 ]
  • [ 1227799-21-4 ]
  • 2
  • [ 563-80-4 ]
  • [ 2243-58-5 ]
  • [ 41532-84-7 ]
YieldReaction ConditionsOperation in experiment
With acetic acid; at 100℃; for 24h; General procedure: In parallel, substituted hydrazines 1 (4.0 g, 22.25 mmol) were reacted with 3-methylbutanone(3 mL, 28.04 mmol) in acetic acid and heated to a 100 C for 24 h. The solution was then neutralizedusing sodium bicarbonate and extracted using dichloromethane; affording substituted indolenineheterocycles 2 which was dried under reduced pressure. The heterocycles 2 were then reacted withan alkyl halide in acetonitrile at 100 C for 12-18 h. The quaternary ammonium salts 3 were precipitatedwith diethyl ether, and collected.
 

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