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Merck

227331

Sigma-Aldrich

2-甲氧基环己酮

97%

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About This Item

线性分子式:
CH3OC6H9(=O)
CAS号:
分子量:
128.17
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

折射率

n20/D 1.455 (lit.)

bp

185 °C/750 mmHg (lit.)

密度

1.02 g/mL at 25 °C (lit.)

官能基

ether
ketone

SMILES 字串

COC1CCCCC1=O

InChI

1S/C7H12O2/c1-9-7-5-3-2-4-6(7)8/h7H,2-5H2,1H3

InChI 密鑰

JYJURPHZXCLFDX-UHFFFAOYSA-N

一般說明

The conformational equilibrium of 2-methoxycyclohexanone was studied by infrared spectroscopy.

應用

2-Methoxycyclohexanone was used in the synthesis of 2-(carbomethoxy)cyclohex-2-en-1-one.

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

156.2 °F - closed cup

閃點(°C)

69 °C - closed cup


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分析证书(COA)

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M P Freitas et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(6), 1177-1182 (2003-03-28)
The conformational equilibrium of 2-methoxycyclohexanone has been analyzed through infrared spectroscopy and theoretical calculations. These calculations indicate that six conformations may be present in the vapor phase, due to the rotation of the methoxy group around the O-C(2) bond, leading
O Hamed et al.
The Journal of organic chemistry, 66(1), 180-185 (2001-06-30)
Unsubstituted or alkyl-substituted cyclic ketones react with PdCl2 in methanol under a CO atmosphere to give mainly acyclic diesters along with some acyclic chloro-substituted monoesters. The monosubstituted cyclic ketones, 2-hydroxy- and 2-methoxycyclohexanone, do not give ring cleavage but rather produce
Qinglei Meng et al.
Nature communications, 8, 14190-14190 (2017-02-01)
Cyclohexanone and its derivatives are very important chemicals, which are currently produced mainly by oxidation of cyclohexane or alkylcyclohexane, hydrogenation of phenols, and alkylation of cyclohexanone. Here we report that bromide salt-modified Pd/C in H

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