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Merck

24-3300

Sigma-Aldrich

Piperidine

SAJ first grade, ≥99.0%

Sinónimos:

Hexahydropyridine

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About This Item

Fórmula empírica (notación de Hill):
C5H11N
Número de CAS:
Peso molecular:
85.15
Beilstein/REAXYS Number:
102438
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:

grade

SAJ first grade

vapor density

3 (vs air)

vapor pressure

23 mmHg ( 20 °C)

assay

≥99.0%

form

liquid

availability

available only in Japan

refractive index

n20/D 1.452 (lit.)

bp

106 °C (lit.)

mp

−13 °C (lit.)

density

0.862 g/mL at 20 °C (lit.)

SMILES string

C1CCNCC1

InChI

1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2

Inchi Key

NQRYJNQNLNOLGT-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

60.8 °F - closed cup

flash_point_c

16 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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A novel series of piperidine-linked amino-triazine derivatives were designed, synthesized and evaluated for in vitro anti-HIV activity as non-nucleoside reverse transcriptase inhibitors on the basis of our previous work. Screening results indicated that most compounds showed excellent activity against wild-type
Elisabeth T Hennessy et al.
Science (New York, N.Y.), 340(6132), 591-595 (2013-05-04)
The manipulation of traditionally unreactive functional groups is of paramount importance in modern chemical synthesis. We have developed an iron-dipyrrinato catalyst that leverages the reactivity of iron-borne metal-ligand multiple bonds to promote the direct amination of aliphatic C-H bonds. Exposure

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