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P46105

Sigma-Aldrich

Piperidine hydrochloride

99%

Synonyma:

Piperidinium chloride

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
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About This Item

Empirický vzorec (Hillův zápis):
C5H11N · HCl
Číslo CAS:
6091-44-7
Molekulová hmotnost:
121.61
Beilstein/REAXYS Number:
3611699
EC Number:
228-033-8
MDL number:
MFCD00012770
UNSPSC Code:
12352100
PubChem Substance ID:
24898558
NACRES:
NA.22

vapor density

2.94 (vs air)

Quality Level

200

vapor pressure

63.6 mmHg ( 37.8 °C)

assay

99%

form

powder

mp

245-248 °C (lit.)

SMILES string

Cl[H].C1CCNCC1

InChI

1S/C5H11N.ClH/c1-2-4-6-5-3-1;/h6H,1-5H2;1H

InChI key

VEIWYFRREFUNRC-UHFFFAOYSA-N

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Související kategorie

Application

Reagent for synthesis of:
  • Quinoline selenium compounds
  • Peripheral seratonin 5-HT3 receptor ligands

Reactant for synthesis of phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors

Reactant for:
  • Mannich reactions
  • Asymmetric hydrogenation of quinolines
  • Chemoselective reductive amination of carbonyl compounds

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Osvědčení o analýze (COA)

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Sigma-Aldrich

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1,3-Dioxolane

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Dimethyl ether ≥99.9%

Sigma-Aldrich

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Sigma-Aldrich

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Syringaldehyde

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Scientific reports, 7, 45364-45364 (2017-03-30)
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A series of novel chroman-4-one derivatives were designed and synthesized successfully with good to excellent yield (3a-l). In addition, the obtained products were evaluated for their cholinesterase (ChE) inhibitory activities. The results show that among the various synthesized compounds, analogs
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Ligands that can interact specifically with telomeric multimeric G-quadruplexes could be developed as promising anticancer drugs with few side effects related to other G-quadruplex-forming regions. In this paper, a new cationic porphyrin derivative, m-TMPipEOPP, was synthesized and characterized. Its multimeric

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