Basic information Safety Supplier Related

1-Boc-2-Methylpiperazine

Basic information Safety Supplier Related

1-Boc-2-Methylpiperazine Basic information

Product Name:
1-Boc-2-Methylpiperazine
Synonyms:
  • N-4-BOC-3-METHYLPIPERIZINE
  • 1-N-Boc-2-methyl-piperizine
  • 2-METHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • (+/-)-1-N-BOC-2-METHYL PIPERAZINE
  • 1-N-BOC-2-METHYLPIPERAZINE
  • TERT-BUTYL 2-METHYLPIPERAZINE-1-CARBOXYLATE
  • TERT-BUTYL-2-METHYL-1-PIPERAZINECARBOXYLATE
  • N-1-BOC-2-METHYLPIPERAZINE
CAS:
120737-78-2
MF:
C10H20N2O2
MW:
200.28
Product Categories:
  • pharmacetical
  • Piperaizine
Mol File:
120737-78-2.mol
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1-Boc-2-Methylpiperazine Chemical Properties

Boiling point:
268.7±15.0 °C(Predicted)
Density 
0.997±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Oil
pka
8.49±0.40(Predicted)
color 
Colourless
CAS DataBase Reference
120737-78-2(CAS DataBase Reference)
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Safety Information

RIDADR 
2735
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2933599590
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1-Boc-2-Methylpiperazine Usage And Synthesis

Uses

tert-Butyl 2-methylpiperazine-1-carboxylate is a useful reagent used in the synthesis of anthrafuran carboxamides with antitumor properties.

Synthesis

120737-77-1

120737-78-2

General procedure for the synthesis of tert-butyl 2-methylpiperazine-1-carboxylate from the compound (CAS: 120737-77-1): a mixture of tert-butyl (RS)-4-benzyl-2-methylpiperazine-1-carboxylate (3.41 g, 11.7 mmol), ethanol (125 mL), and Pearlman's catalyst (0.854 g, 6.08 mmol) was was hydrogenated overnight at 36 psi pressure at ambient temperature. Upon completion of the reaction, the mixture was filtered and the solids were washed sequentially with ethanol, dichloromethane (DCM) and methanol (MeOH). The filtrate and washings were combined, concentrated in vacuum, redissolved in dichloromethane, filtered again and concentrated in vacuum to give tert-butyl 2-methylpiperazine-1-carboxylate as a beige oil (2.0 g, 86% yield). The nuclear magnetic resonance (NMR) spectrum of the product was in agreement with the data reported in the literature (J. Org. Chem. 1995, 60, 4183).

References

[1] Patent: WO2007/135427, 2007, A1. Location in patent: Page/Page column 31
[2] Patent: US4880808, 1989, A

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