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Chemical Structure| 163765-44-4 Chemical Structure| 163765-44-4
Chemical Structure| 163765-44-4

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Product Details of (R)-1-Boc-3-methyl-piperazine

CAS No. :163765-44-4
Formula : C10H20N2O2
M.W : 200.28
SMILES Code : [C@@H]1(NCCN(C(OC(C)(C)C)=O)C1)C
MDL No. :MFCD02683205
InChI Key :FMLPQHJYUZTHQS-MRVPVSSYSA-N
Pubchem ID :2756811

Safety of (R)-1-Boc-3-methyl-piperazine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of (R)-1-Boc-3-methyl-piperazine

* 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 [ 163765-44-4 ]

[ 163765-44-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 2895-21-8 ]
  • [ 163765-44-4 ]
  • C10H21N3O*2ClH [ No CAS ]
  • 2
  • [ 2895-21-8 ]
  • [ 163765-44-4 ]
  • C15H29N3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
711 mg With sodium carbonate; In acetonitrile; at 60℃; for 18h; (1) The compound 1 (500 mg), the compound 2 (677 mg) and sodium carbonate (529 mg) were suspended inacetonitrile (10 mL), and the reaction mixture was stirred for 18 hours at 60 C. The reaction mixture was cooled toroom temperature, and then diluted with ethyl acetate, washed with water and brine, and dried over anhydroussodium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified by silicagel column chromatography (eluent: ethyl acetate-methanol; gradient: 100:0-95:5) to give the compound 3 (711 mg)as a colorless solid.MS (APCI) 300 [M+H]+
  • 3
  • [ 902586-59-8 ]
  • [ 163765-44-4 ]
  • propyl (R)-4-(9-chloro-5,6,7,8-tetrahydroacridine-3-carbonyl)-3-methylpiperazine-1-carboxylate [ No CAS ]
  • 4
  • [ 902586-59-8 ]
  • [ 163765-44-4 ]
  • tert-butyl 4-(9-chloro-5,6,7,8-tetrahydroacridine-3-carbonyl)-3-methylpiperazine-1-carboxylate [ No CAS ]
 

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