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[ CAS No. 40432-40-4 ] {[proInfo.proName]}

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Chemical Structure| 40432-40-4
Chemical Structure| 40432-40-4
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Product Details of [ 40432-40-4 ]

CAS No. :40432-40-4 MDL No. :MFCD06658337
Formula : C11H14N2O Boiling Point : -
Linear Structure Formula :- InChI Key :NYSSYUHBYRIDQA-UHFFFAOYSA-N
M.W : 190.24 Pubchem ID :10932239
Synonyms :

Safety of [ 40432-40-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280 UN#:N/A
Hazard Statements:H302-H317 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 40432-40-4 ]

* 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 [ 40432-40-4 ]

[ 40432-40-4 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 18085-37-5 ]
  • [ 40432-40-4 ]
  • 3
  • [ 40432-40-4 ]
  • [ 46193-94-6 ]
YieldReaction ConditionsOperation in experiment
With borane-THF 1.) THF, a) RT, 2 h, b) reflux, 8 h, 2.) EtOH, reflux, 2 h; Yield given. Multistep reaction;
  • 5
  • [ 40432-40-4 ]
  • [ 209607-03-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 2: 1.) BH3*THF / 1.) THF, a) RT, 2 h, b) reflux, 8 h, 2.) EtOH, reflux, 2 h
  • 6
  • [ 40432-40-4 ]
  • [ 209607-02-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 2: 1.) BH3*THF / 1.) THF, a) RT, 2 h, b) reflux, 8 h, 2.) EtOH, reflux, 2 h
  • 7
  • [ 40432-40-4 ]
  • (S)-N-((S)-1-Benzyl-azetidin-2-ylmethyl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 2: 1.) BH3*THF / 1.) THF, a) RT, 2 h, b) reflux, 8 h, 2.) EtOH, reflux, 2 h 3: 1.) pyridine / 1.) CH2Cl2, RT, 3 h, 2.) CH2Cl2, RT, 3.5 h
  • 8
  • [ 40432-40-4 ]
  • (S)-N-((R)-1-Benzyl-azetidin-2-ylmethyl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 2: 1.) BH3*THF / 1.) THF, a) RT, 2 h, b) reflux, 8 h, 2.) EtOH, reflux, 2 h 3: 1.) pyridine / 1.) CH2Cl2, RT, 3 h, 2.) CH2Cl2, RT, 3.5 h
  • 9
  • [ 100-46-9 ]
  • [ 40432-40-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 45 percent / K2CO3 / acetonitrile; H2O / Heating 2: 81 percent / conc. aq. NH3 / 3 h
  • 10
  • [ 40432-40-4 ]
  • (2R)-N-benzylazetidine-2-carboxylic acid [ No CAS ]
  • [ 205443-26-1 ]
YieldReaction ConditionsOperation in experiment
49% With Rhodococcus erythropolis AJ270 at 30℃; for 3.7h; aq. phosphate buffer; Enzymatic reaction; optical yield given as %ee; enantioselective reaction;
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