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Chemical Structure| 42558-54-3 Chemical Structure| 42558-54-3
Chemical Structure| 42558-54-3

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Product Details of Methyl 4-methyl-3-oxovalerate

CAS No. :42558-54-3
Formula : C7H12O3
M.W : 144.17
SMILES Code : CC(C(CC(=O)OC)=O)C
MDL No. :MFCD00040499
InChI Key :HNNFDXWDCFCVDM-UHFFFAOYSA-N
Pubchem ID :2759969

Safety of Methyl 4-methyl-3-oxovalerate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H227-H315-H319-H335
Precautionary Statements:P305+P351+P338

Application In Synthesis of Methyl 4-methyl-3-oxovalerate

* 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 [ 42558-54-3 ]

[ 42558-54-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 42558-54-3 ]
  • [ 25185-95-9 ]
  • [ 278597-28-7 ]
  • 2
  • [ 757251-39-1 ]
  • [ 42558-54-3 ]
  • [ 320-51-4 ]
  • [ 755037-03-7 ]
YieldReaction ConditionsOperation in experiment
96.8% With dmap; In N,N-dimethyl-formamide; at 140℃; for 4h;Green chemistry; To the reaction flask, a compound IV 13.27 g, a compound V 9.93 g, a methyl isobutyryl acetate 7.32 g, a 4-dimethylaminopyridine 6.21 g, and 800 ml of DMF were sequentially added, and the mixture was stirred and dissolved, and the temperature was controlled at 140 C for 4 h. The TLC monitors the completion of the reaction. The reaction was stopped, the temperature was lowered to room temperature, and ethyl acetate was added for extraction. The organic layer was separated and concentrated under reduced pressure to give 25.55 g, product yield 96.8%, purity 99.93%.
  • 3
  • [ 120-72-9 ]
  • [ 42558-54-3 ]
  • [ 621-63-6 ]
  • methyl 4-(1H-indol-3-yl)-2-isopropyl-4,5-dihydrofuran-3-carboxylate [ No CAS ]
 

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