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Merck
CN

80630

Supelco

哌嗪 六水合物

≥98.0% (T)

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About This Item

经验公式(希尔记法):
C4H10N2 · 6H2O
CAS号:
分子量:
194.23
Beilstein:
4455527
EC 号:
MDL编号:
UNSPSC代码:
12000000

蒸汽压

0.8 mmHg ( 20 °C)

方案

≥98.0% (T)

沸点

145-156 °C (lit.)

mp

42-44 °C (lit.)
42-44 °C

SMILES字符串

[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

InChI key

AVRVZRUEXIEGMP-UHFFFAOYSA-N

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Yinghui Mo et al.
Environmental science & technology, 46(24), 13253-13261 (2012-12-05)
Carboxyls are inherent functional groups of thin-film composite polyamide nanofiltration (NF) membranes, which may play a role in membrane performance and fouling. Their surface presence is attributed to incomplete reaction of acyl chloride monomers during the membrane active layer synthesis
Girish D Hatnapure et al.
Bioorganic & medicinal chemistry letters, 22(20), 6385-6390 (2012-09-18)
A series of novel 6-methoxy-2-(piperazin-1-yl)-4H-chromen-4-one and 5,7-dimethoxy-2-(piperazin-1-ylmethyl)-4H-chromen-4-one derivatives of biological interest were prepared and screened for their pro-inflammatory cytokines (TNF-α and IL-6) and antimicrobial activity (antibacterial and antifungal). Among all the compound screened (5a-j and 10k-t), the compounds 5c, 5g
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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
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
Jadwiga Handzlik et al.
Bioorganic & medicinal chemistry, 20(14), 4245-4257 (2012-06-29)
The study is focused on a series of 5-arylidenehydantoin derivatives with a phenylpiperazine-hydroxypropyl fragment at N3 of the hydantoin ring. The compounds were assessed on their affinity for α(1)-adrenoceptors and evaluated in functional bioassays for their antagonistic properties. Crystal structures

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