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Merck
CN

29620

环辛酮

purum, ≥95.0% (GC)

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关于此项目

线性分子式:
C8H14(=O)
化学文摘社编号:
分子量:
126.20
EC Number:
207-940-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1280738
MDL number:
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grade

purum

assay

≥95.0% (GC)

bp

195-197 °C (lit.)

mp

32-41 °C (lit.)

solubility

methanol: soluble 1 g/10 mL, clear to very faintly turbid, colorless

density

0.958 g/mL at 25 °C (lit.)

SMILES string

O=C1CCCCCCC1

InChI

1S/C8H14O/c9-8-6-4-2-1-3-5-7-8/h1-7H2

InChI key

IIRFCWANHMSDCG-UHFFFAOYSA-N

General description

Phase transition from liquid to disordered (plastic) solid phase of cyclooctanone has been studied by dielectric methods.

Application

Cyclooctanone has been used in the preparation of:
  • sulfonylbicyclo[3.2.0]heptan-1-ols, sulfonylbicyclo[5.2.0]-nonan-1-ols and sulfonylbicyclo[6.2.0]decan-1-ols
  • 14-membered lactones

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

165.2 °F

flash_point_c

74 °C

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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Jolanta Swiergiel et al.
The journal of physical chemistry. B, 116(12), 3789-3794 (2012-03-08)
The dielectric studies performed for cyclooctanone in its static dielectric regime have shown that at the phase transition from liquid to disordered (plastic) solid phase of the compound, the following singular phenomena occur: (a) the static permittivity (ε(s)) exhibits a
Synthesis of 14-Membered Lactones from Cyclooctanone.
Aono T and Hesse T.
Helvetica Chimica Acta, 67(6), 1448-1452 (1984)
K Yamada et al.
Chemical & pharmaceutical bulletin, 45(12), 1898-1905 (1998-01-20)
Construction of the AB-ring system of the taxane framework via an A-ring annulation strategy was demonstrated by base-mediated intramolecular aldol reaction of (Z)-2,2-dimethyl-3-(1-methyl-2-oxopropylidene)cyclooctanone, affording the title compound, 1-hydroxy-8,11,11-trimethylbicyclo[5.3.1]undec-7-en-9-one. A cyclization precursor, the tetra-substituted (Z)-alkene, was prepared from the corresponding cyclooctanone
Vishwakarma Singh et al.
The Journal of organic chemistry, 70(3), 973-981 (2005-01-29)
A new and efficient synthesis of a variety of highly embellished bicyclooctenones having an endo-vinyl moiety and their sigmatropic shifts in ground and excited states leading to a stereoselective route to substituted cis-decalins and diquinane frameworks have been described. Functionalized
F E Harvey et al.
Brain research bulletin, 13(4), 541-547 (1984-10-01)
Female mice were reared in observation incubators from day 1 of life for three weeks. During that time they were continuously exposed to the odors of either cyclooctanone, adult male mouse urine or distilled water. The growth rate was temporarily

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