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Chemical Structure| 19788-35-3 Chemical Structure| 19788-35-3

Structure of 19788-35-3

Chemical Structure| 19788-35-3

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Product Details of [ 19788-35-3 ]

CAS No. :19788-35-3
Formula : C6H7NO3
M.W : 141.12
SMILES Code : O=C(C1=NOC(C)=C1)OC
MDL No. :MFCD00015895
InChI Key :MVHHQOCEOUNTID-UHFFFAOYSA-N
Pubchem ID :88245

Safety of [ 19788-35-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 19788-35-3 ]

* 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.

  • Upstream synthesis route of [ 19788-35-3 ]
  • Downstream synthetic route of [ 19788-35-3 ]

[ 19788-35-3 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 19788-35-3 ]
  • [ 850832-54-1 ]
YieldReaction ConditionsOperation in experiment
60% With bromine In chloroform for 3 h; Heating / reflux Bromine (49.4g, 309mmol) was added to a solution of methyl 5-methylisoxazole-3-carboxylate (30g, 206mmol) in chloroform (103ml) at room temperature and the mixture was refluxed for 3 hours. After cooling, the reaction mixture was poured into a saturated aqueous potassium carbonate- saturated aqueous sodium thiosulfate and extracted with chloroform twice. The combined organic layer was washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane: ethyl acetate = 10: 1) to give methyl 4-bromo-5-methylisoxazole-3-carboxylate (27. 3g, 60percent) as a solid. MS: 220/222 [M+H] +, APCI (MeOH)
References: [1] Patent: WO2005/37271, 2005, A2, . Location in patent: Page/Page column 185.
[2] Journal of Medicinal Chemistry, 2018, vol. 61, # 18, p. 8337 - 8352.
 

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[ 19788-35-3 ]

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