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80630

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Piperazine hexahydrate

≥98.0% (T)

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About This Item

Fórmula empírica (notación de Hill):
C4H10N2 · 6H2O
Número de CAS:
142-63-2
Peso molecular:
194.23
Beilstein:
4455527
Número CE:
203-808-3
Número MDL:
MFCD00149389
Código UNSPSC:
12000000

presión de vapor

0.8 mmHg ( 20 °C)

Ensayo

≥98.0% (T)

bp

145-156 °C (lit.)

mp

42-44 °C (lit.)
42-44 °C

cadena SMILES

[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].C1CNCCN1

InChI

1S/C4H10N2.6H2O/c1-2-6-4-3-5-1;;;;;;/h5-6H,1-4H2;6*1H2

Clave InChI

AVRVZRUEXIEGMP-UHFFFAOYSA-N

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P7003

Piperazine hexahydrate, analytical standard

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P Krishnan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 102, 379-385 (2012-12-12)
Monohydrate piperazine hydrogen phosphate (MPHP), a semi organic nonlinear optical material has been synthesized and single crystals were grown from aqueous solution by slow evaporation technique. Single crystal X-ray diffraction study on grown crystal reveals that they belong to monoclinic
Leila Hassanzadeh et al.
Nuclear medicine and biology, 40(2), 227-232 (2012-11-13)
It has been recognized that serotonin plays a main role in various pathological conditions such as anxiety, depression, aggressiveness, schizophrenia, suicidal behavior, panic and autism. 1-(2-Methoxyphenyl) piperazine pharmacophore, a fragment of the true 5-HT(1A) antagonist WAY100635, is found in numerous
Slavka Hamulakova et al.
European journal of medicinal chemistry, 55, 23-31 (2012-07-24)
New tacrine derivatives 5a-d, 6a-d with piperazino-ethyl spacer linked with corresponding secondary amines and tacrine homodimer 8 were synthesized and tested as cholinesterase inhibitors on human acetylcholinesterase (hAChE) and human plasmatic butyrylcholinesterase (hBChE). In most cases the majority of synthesized
Jung-Eun Park et al.
Bioorganic & medicinal chemistry letters, 23(6), 1887-1890 (2013-02-12)
To obtain selective and potent inhibitor for T-type calcium channel by ligand based drug design, 2-hydroxy-3-phenoxypropyl piperazine derivatives were synthesized and evaluated for in vitro activities. Compound 6m and 6q showed high selectivity over hERG channel (IC50 ratio of hERG/α1G6m=8.5
Enza Lacivita et al.
Journal of medicinal chemistry, 55(14), 6375-6380 (2012-06-29)
Here we report the design, synthesis, and 5-HT(7) receptor affinity of a set of 1-(3-biphenyl)- and 1-(2-biphenyl)piperazines. The effect on 5-HT(7) affinity of various substituents on the second (distal) phenyl ring was analyzed. Several compounds showed 5-HT(7) affinities in the
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