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Manufacturer Supply High Quality CAS 57260-71-6 Tert-Butyl 1-Piperazinecarboxylate
Model NO.
TY-02AL
Colour
White
Package
Foil Bag
Place
China
Assay
99%
Shelf
2 Years
Transport Package
25kg/Drum 5g, 100g, 500g, 1kg, 10kg, 100kg, 200kg
Specification
25kg/drum
Trademark
tongyon
Origin
China
Production Capacity
5000kg/Month
Reference Price
Please contact us for quote
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Description
Product Description
Product name
tert-Butyl 1-piperazinecarboxylate
CAS
57260-71-6
Appearance
white powder
Assay
99%
Storage
Cool and Protect from light
tert-Butyl 1-piperazinecarboxylate
Product Name tert-Butyl 1-piperazinecarboxylate
CAS 57260-71-6
MF C9H18N2O2
MW 186.25
EINECS 611-489-0
MOL File 57260-71-6.mol
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
pka 8.45±0.10(Predicted)
form Low Melting Crystalline Mass
color White to light yellow
Water Solubility Soluble in ethyl acetatee, methanoll 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)
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
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.
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