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Chemical Structure| 17610-21-8 Chemical Structure| 17610-21-8

Structure of 17610-21-8

Chemical Structure| 17610-21-8

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Product Details of [ 17610-21-8 ]

CAS No. :17610-21-8
Formula : C16H22O
M.W : 230.35
SMILES Code : CC(=O)C1=CC2=C(C=C1)C(C)(C)CCC2(C)C
MDL No. :MFCD00052727
InChI Key :IHUSZOMIBSDQTB-UHFFFAOYSA-N
Pubchem ID :2747562

Safety of [ 17610-21-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 17610-21-8 ]

* 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 [ 17610-21-8 ]

[ 17610-21-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4565-31-5 ]
  • [ 17610-21-8 ]
  • [ 241140-20-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; sodium hydroxide; In methanol; b. Preparation of 5-[(E)-3-oxo-3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-yl)propenyl]thiophene-2-carboxylic acid: 2.3 g (10 mmol) of 1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)ethanone and 1.7 g (10 mmol) of 5-formylthiophene-2-carboxylic acid are dissolved in 70 ml of methanol. 40 ml of a 1N sodium hydroxide solution are added and the reaction mixture is stirred for 48 hours at ambient temperature. The mixture is acidified by addition of hydrochloric acid and then the mixture is extracted with ethyl ether. The residue is recrystallized from ether (M.p.=204° C., m=2 g, Y=54percent).
 

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