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Chemical Structure| 2687-12-9 Chemical Structure| 2687-12-9
Chemical Structure| 2687-12-9

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Product Details of (3-Chloroprop-1-en-1-yl)benzene

CAS No. :2687-12-9
Formula : C9H9Cl
M.W : 152.62
SMILES Code : ClCC=CC1=CC=CC=C1
MDL No. :MFCD00000986

Safety of (3-Chloroprop-1-en-1-yl)benzene

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314-H330-H334
Precautionary Statements:P260-P280-P284-P305+P351+P338-P310
Class:8(6.1)
UN#:2922
Packing Group:

Application In Synthesis of (3-Chloroprop-1-en-1-yl)benzene

* 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 [ 2687-12-9 ]

[ 2687-12-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 21252-69-7 ]
  • [ 2687-12-9 ]
  • 1-octyl-3-cinnamylimidazolium chloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% In neat (no solvent); at 80℃; for 0.0833333h;Microwave irradiation; Green chemistry; General procedure: Briefly, a mixture of alkylimidazoles such as 1-methyl-1H-imidazole (MIM), 1-hexyl-1H-imidazole(HIM), <strong>[21252-69-7]1-octyl-1H-imidazole</strong> (OIM), and 1-decyl-1H-imidazole (DIM) (1 mmol), as well as cinnamylchloride (1 mmol) solvent-free were microwaved to 200 MW at 80 C for 5 min (optimumreaction condition). Reaction completion was marked by separation of dense IL. Products suchas 1-methyl-3-cinnamylimidazolium chloride [CMIM]Cl, 1-hexyl-3-cinnamylimidazolium chloride[CHIM]Cl, 1-octyl-3-cinnamylimidazolium chloride [COIM]Cl, and 1-decyl-3-cinnamylimidazolium chloride [CDIM]Cl were isolated by decanting toluene to remove any unreacted starting materialsand solvents. Subsequently, ILs were rinsed with diethyl ether (4 10 mL) separating afterward thislatter layer by decantation. In each case, ILs were finally dried under reduced pressure to get rid of thevolatile organic compounds.
 

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