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1-BOC-Piperazine

Basic information Uses Safety Supplier Related

1-BOC-Piperazine Basic information

Product Name:
1-BOC-Piperazine
Synonyms:
  • 1-Boc-piperazine,99%
  • 1-(tert-Butyloxycarbonyl)piperazine
  • 1-Piperazinecarboxylic Acid 1,1-Dimethylethyl Ester
  • 1-Piperazinecarboxylic Acid tert-Butyl Este
  • N-(tert-Butoxycarbonyl)piperazine 98%
  • Piperazine, N1-BOC protected
  • tert-Butyl 2-piperazinecarboxylate
  • N-(T-BUTYLOXYCARBONYL)-PIPERAZINE
CAS:
57260-71-6
MF:
C9H18N2O2
MW:
186.25
EINECS:
611-489-0
Product Categories:
  • Building Blocks
  • C9
  • Piperidines, Piperidones, Piperazines
  • Heterocyclic Compounds
  • Miscellaneous Reagents
  • Pyrans, Piperidines & Piperazines
  • Amines and Anilines
  • pharmacetical
  • PiperazineDerivative
  • Pyrans, Piperidines &Piperazines
  • Piperaizine
  • Piperazines
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Heterocycles
  • 1
  • 57260-71-6
  • john's
Mol File:
57260-71-6.mol
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1-BOC-Piperazine Chemical Properties

Melting point:
43-47 °C(lit.)
Boiling point:
98-100
Density 
1.030±0.06 g/cm3(Predicted)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
Soluble in DMSO
pka
8.45±0.10(Predicted)
form 
Low Melting Crystalline Mass
color 
White to light yellow
Water Solubility 
Soluble in ethyl acetate, methanol and water.
Sensitive 
Air Sensitive
BRN 
879985
InChIKey
CWXPZXBSDSIRCS-UHFFFAOYSA-N
CAS DataBase Reference
57260-71-6(CAS DataBase Reference)
NIST Chemistry Reference
T-butyl 1-piperaziencarboxylate(57260-71-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
3263
WGK Germany 
3
3-10-34
HazardClass 
IRRITANT
HS Code 
29335995

MSDS

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1-BOC-Piperazine Usage And Synthesis

Uses

N-Boc-piperazine is a compound useful in organic synthesis.

Chemical Properties

Waxy Solid

Uses

1-Boc-piperazine undergoes Buchwald-Hartwig amination with various aryl halides to form corresponding amine derivatives. It can be used to synthesize monosubstituted piperazine intermediates of many bioactive molecules and piperazine containing drug substances, such as trazodone.

Uses

1-Boc-piperazine may be used in:

  • preparation of series of (m-phenoxy)phenyl substituted piperazine derivatives
  • termination step during synthesis of α,β-poly(2-oxazoline) lipopolymers via living cationic ring opening polymerization
  • preparation of monosubstituted piperazines, e.g. in the synthesis of indazole DNA gyrase inhibitors

Application

Tert-Butyl 1-piperazinecarboxylate, also known as Olaparib Impurity 7, is an impurity of Olaparib. Olaparib is used alone or in combination with bevacizumab (Avastin) to help maintain the response of certain types of ovarian (female reproductive organs where eggs are formed), fallopian tube (tube that transports eggs released by the ovaries to the uterus), and peritoneal (layer of tissue that lines the abdomen) cancer in people who have completely responded or partially responded to their first or later chemotherapy treatments. Olaparib is also used to treat certain types of breast cancer that has spread to other parts of the body and has not improved or has worsened after treatment with other therapies. It is also used to treat certain types of early breast cancer in people who have already been treated with other chemotherapy treatments.

General Description

1-Boc-piperazine is an N-Boc protected piperazine. Crosscoupling of 1-Boc-piperazine with aryl iodides using CuBr/1,1′-bi-2-naphthol (catalyst) and K3PO4 (base) has been reported. 1-Boc-piperazine undergoes Buchwald-Hartwig coupling reactions with aryl halides. 1-Boc-piperazine can be prepared in 80% yield via solvent-free N-Boc protection catalyzed by iodine.

1-BOC-Piperazine Supplier

Hubei Jingxiang Technology Co., Ltd. Gold
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Anhui Dexinjia Biopharm Co., Ltd Gold
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0531-82375878 15269101859
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Chengdu Firster Pharmaceutical Co., Ltd. Gold
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028-87078428 028-87074958
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Nantong Jiaxingtai Biotechnology Co., Ltd. Gold
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18795782766
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Zhejiang Aobang Pharmaceutical & Chemical Co. LTD Gold
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13676682222 13676682222
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