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[ CAS No. 497107-76-3 ] {[proInfo.proName]}

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Chemical Structure| 497107-76-3
Chemical Structure| 497107-76-3
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Product Details of [ 497107-76-3 ]

CAS No. :497107-76-3 MDL No. :MFCD24466945
Formula : C11H21NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :DNACUGFUHHLHTJ-UHFFFAOYSA-N
M.W : 215.29 Pubchem ID :11321865
Synonyms :

Safety of [ 497107-76-3 ]

Signal Word:Warning Class:N/A
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 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 497107-76-3 ]

* 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 [ 497107-76-3 ]

[ 497107-76-3 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 75-77-4 ]
  • [ 497107-76-3 ]
  • Methyl-[3-((2S,3S)-3-trimethylsilanyl-oxiranyl)-propyl]-carbamic acid tert-butyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% With 2,2,6,6-tetramethylpiperidinyl-lithium In tetrahydrofuran; hexane at 0℃; for 6h;
  • 2
  • tert-butyl N-methyl-N-(pent-4-en-1-yl)carbamate [ No CAS ]
  • [ 497107-76-3 ]
YieldReaction ConditionsOperation in experiment
79% With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 20℃; for 4h;
  • 3
  • [ 768-66-1 ]
  • [ 497107-76-3 ]
  • 1-(5-N-Boc-N-methylaminopent-1-enyl)-2,2,6,6-tetramethylpiperidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
63% Stage #1: 2,2,6,6-tetramethyl-piperidine With n-butyllithium In tetrahydrofuran; hexane at 0 - 25℃; for 0.25h; Stage #2: 5-(N-Boc-N-methylamino)-1,2-epoxypentane In tetrahydrofuran; hexane at 25℃; for 1h;
  • 4
  • [ 51779-32-9 ]
  • [ 497107-76-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 75 percent / NaH / tetrahydrofuran; dimethylformamide / 6 h / 70 °C 2: 69 percent / TFA / CH2Cl2 / 20 h / 20 °C 3: 76 percent / NaH / tetrahydrofuran; dimethylformamide / 20 h / 20 °C 4: 79 percent / mCPBA / CH2Cl2 / 4 h / 20 °C
  • 5
  • [ 1119-51-3 ]
  • [ 497107-76-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 75 percent / NaH / tetrahydrofuran; dimethylformamide / 6 h / 70 °C 2: 69 percent / TFA / CH2Cl2 / 20 h / 20 °C 3: 76 percent / NaH / tetrahydrofuran; dimethylformamide / 20 h / 20 °C 4: 79 percent / mCPBA / CH2Cl2 / 4 h / 20 °C
  • 6
  • [ 202925-92-6 ]
  • [ 497107-76-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 76 percent / NaH / tetrahydrofuran; dimethylformamide / 20 h / 20 °C 2: 79 percent / mCPBA / CH2Cl2 / 4 h / 20 °C
  • 7
  • [ 562064-07-7 ]
  • [ 497107-76-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 69 percent / TFA / CH2Cl2 / 20 h / 20 °C 2: 76 percent / NaH / tetrahydrofuran; dimethylformamide / 20 h / 20 °C 3: 79 percent / mCPBA / CH2Cl2 / 4 h / 20 °C
  • 8
  • [ 768-66-1 ]
  • [ 497107-76-3 ]
  • 1-(5-N-Boc-N-methylaminopent-1-enyl)-2,2,6,6-tetramethylpiperidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
63% Stage #1: 2,2,6,6-tetramethyl-piperidine With n-butyllithium In tetrahydrofuran at 0 - 25℃; for 0.25h; Stage #2: 5-(N-Boc-N-methylamino)-1,2-epoxypentane In tetrahydrofuran at 25℃; for 1h;
  • 9
  • [ 873869-19-3 ]
  • [ 497107-76-3 ]
  • tert-butyl (4-(2,2-dioxo-1,2-oxathiolan-5-yl)propyl)(methyl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
48% With lithium hexamethyldisilazane In hexane; dichloromethane at 20 - 25℃; for 20h;
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