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Chemical Structure| 1075-47-4 Chemical Structure| 1075-47-4

Structure of 1075-47-4

Chemical Structure| 1075-47-4

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Product Details of [ 1075-47-4 ]

CAS No. :1075-47-4
Formula : C9H8O2
M.W : 148.16
SMILES Code : O=CC(C1=CC=C(C)C=C1)=O
MDL No. :MFCD00235014

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Application In Synthesis of [ 1075-47-4 ]

* 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 [ 1075-47-4 ]

[ 1075-47-4 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 1075-47-4 ]
  • [ 10167-97-2 ]
  • 6-Methoxy-2-p-tolyl-imidazo[1,2-a]pyridin-3-ol [ No CAS ]
  • 2
  • [ 139016-20-9 ]
  • [ 1075-47-4 ]
  • [ 4079-54-3 ]
  • 3
  • [ 1075-47-4 ]
  • [ 7466-72-0 ]
  • [ 99651-34-0 ]
  • Allyl 6-Bromo-6-[1-hydroxy-2-(4-methylphenyl)-2-oxoethyl]penicillanate [ No CAS ]
YieldReaction ConditionsOperation in experiment
In toluene; EXAMPLE A22 Allyl 6-Bromo-6-[1-hydroxy-2-(4-methylphenyl)-2-oxoethyl]penicillanate <strong>[7466-72-0](4-Methylphenyl)glyoxal hydrate</strong> (3.5 g.) was distilled in a Kugelrohr apparatus (105°, 0.75 mm) to yield 2.0 g. (0.0135 mol) of (4-methylphenyl)glyoxal which was immediately dissolved in 25 ml. of toluene and reacted with allyl 6,6-dibromopenicillanate (5.38 g., 0.0135 mol) concurrently converted to the Grignard according to Example A14. After 1.5 hours at -78°, the reaction was quenched and product isolated according to Example A20 to yield crude title product as an oil, tlc Rf 0.27 and 0.32 (4:1 hexane:ethyl acetate), reflecting side chain epimers.
  • 5
  • [ 590-92-1 ]
  • [ 1075-47-4 ]
  • [ 931-53-3 ]
  • [ 24835-08-3 ]
  • 5-(N-cyclohexylcarbamoyl)-5-(4-methylbenzoyl)-1-(2-nitrobenzyl)-2-pyrrolidinone [ No CAS ]
 

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