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Chemical Structure| 68857-86-3 Chemical Structure| 68857-86-3

Structure of 68857-86-3

Chemical Structure| 68857-86-3

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Product Details of [ 68857-86-3 ]

CAS No. :68857-86-3
Formula : C12H16O
M.W : 176.25
SMILES Code : CC(C(C1=CC=C(C=C1)CC)=O)C
MDL No. :MFCD08457175
InChI Key :UFZXPKYGNCVADM-UHFFFAOYSA-N
Pubchem ID :13570280

Safety of [ 68857-86-3 ]

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 [ 68857-86-3 ]

* 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 [ 68857-86-3 ]

[ 68857-86-3 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 68857-86-3 ]
  • [ 920-39-8 ]
  • 3-(4-ethyl-phenyl)-2,4-dimethyl-pentan-3-ol [ No CAS ]
  • 2
  • [ 68857-86-3 ]
  • [ 100319-40-2 ]
  • 3
  • [ 100-41-4 ]
  • [ 79-30-1 ]
  • [ 68857-86-3 ]
  • 4
  • [ 598-26-5 ]
  • [ 100-41-4 ]
  • [ 68857-86-3 ]
  • 7
  • [ 68857-86-3 ]
  • [ 618-40-6 ]
  • 2-(4-ethylphenyl)-1,3,3-trimethyl-3H-indolium perchlorate [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% EXAMPLE V Preparation of 6-acetyl-1-isopropyl-5-ethyl-2,3,3-trimethyl indan according to the reaction schemes of FIG. 1 and FIG. 8 At 10 C. a solution of 93 g (0.72 mol) AlCl3 in 250 ml nitromethane is added to a mixture of 66 g (0.62 mol) ethyl benzene and 70 g (0.66 mol) isobutyroyl chloride, after which the mixture is stirred during half an hour. The reaction mixture is poured out into ice and extracted with ether. The solution in ether is washed neutral, dried on MgSO4 and evaporated. The residue is distilled under diminished pressure to obtain p-ethylphenyl isopropyl ketone in a yield of 77%.
  • 9
  • [ 110-89-4 ]
  • [ 68857-86-3 ]
  • 1-(4-ethylphenyl)-2,2-dimethyl-3-piperidinopropan-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; paraformaldehyde; In water; (6) Preparation of 1-(4-ethylphenyl)-2,2-dimethyl-3-piperidinopropan-1-one (compound 6): A mixture of 18.0 g (0.102 mol) of <strong>[68857-86-3]1-(4-ethylphenyl)-2-methylpropan-1-one</strong>, 15.0 g of paraformaldehyde, 8.5 g (0.10 mol) of piperidine and 10 ml of hydrochloric acid was stirred overnight with heating in an oil bath set to 110 C. After cooling, water was added thereto. After washing with ether and neutralization with alkali, it was extracted with ether. The ether was then evaporated, and the residue was purified by column chromatography. Yellow oil.
  • 10
  • [ 68857-86-3 ]
  • [ 171364-80-0 ]
  • methyl 5'-ethyl-2'-isobutyrylbiphenyl-4-carboxylate [ No CAS ]
  • 11
  • [ 937-30-4 ]
  • [ 74-88-4 ]
  • [ 68857-86-3 ]
  • 12
  • [ 67-56-1 ]
  • 1-(4-ethyl phenyl)prop-2-en-1-ol [ No CAS ]
  • [ 68857-86-3 ]
  • 13
  • [ 4748-78-1 ]
  • [ 68857-86-3 ]
 

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