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Merck

C98403

Sigma-Aldrich

Cycloheptane

98%

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About This Item

Fórmula empírica (notación de Hill):
C7H14
Número de CAS:
Peso molecular:
98.19
Beilstein/REAXYS Number:
1900279
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

44 mmHg ( 37.7 °C)

Quality Level

assay

98%

form

liquid

refractive index

n20/D 1.445 (lit.)

bp

118.5 °C (lit.)

mp

−12 °C (lit.)

density

0.811 g/mL at 25 °C (lit.)

SMILES string

C1CCCCCC1

InChI

1S/C7H14/c1-2-4-6-7-5-3-1/h1-7H2

InChI key

DMEGYFMYUHOHGS-UHFFFAOYSA-N

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pictograms

FlameHealth hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

42.8 °F - closed cup

flash_point_c

6 °C - closed cup

ppe

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


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Jossue Ortiz-Álvarez et al.
Journal of basic microbiology, 59(8), 792-806 (2019-08-02)
The aim of this study was to examine four strains of two yeast species in relation to their capability for assimilating alkanes in the presence of heavy metals (HMs). The four strains tested were Candida pseudoglaebosa ENCB-7 and Kodamaea ohmeri
Chris E Freye et al.
Talanta, 211, 120668-120668 (2020-02-20)
The ability to discover minute differences between samples or sample classes for gas chromatography coupled to mass spectrometry (GC-MS) can be a challenging endeavor, especially when those differences are not a priori. Fisher ratio (F-ratio) analysis is an apt technique
Amanda L Pitts et al.
Journal of the American Chemical Society, 136(24), 8614-8625 (2014-05-16)
Carbon-hydrogen bond activation reactions of four cycloalkanes (C5H10, C6H12, C7H14, and C8H16) by the Cp'Rh(CO) fragments (Cp' = η(5)-C5H5 (Cp) or η(5)-C5Me5 (Cp*)) were modeled theoretically by combining density functional and coupled cluster theories, and their reaction rates were measured
Michael H Abraham et al.
European journal of medicinal chemistry, 44(2), 885-890 (2008-07-08)
The convulsant activity of 48 compounds studied by Eger et al. has been analyzed using an Abraham solvation equation. Four compounds identified by Eger et al. as more potent than expected were similarly identified, and for the remaining 44 compounds
A A Toropov et al.
European journal of medicinal chemistry, 43(4), 714-740 (2007-07-17)
Simplified molecular input line entry system (SMILES) has been utilized in constructing quantitative structure-property relationships (QSPR) for octanol/water partition coefficient of vitamins and organic compounds of different classes by optimal descriptors. Statistical characteristics of the best model (vitamins) are the

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