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Merck

405760

Sigma-Aldrich

2-氧-1-环辛烷羧酸乙酯

97%

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About This Item

线性分子式:
(O=)C8H13CO2C2H5
CAS号:
分子量:
196.24
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

liquid

折射率

n20/D 1.483 (lit.)

bp

85-87 °C/0.1 mmHg (lit.)

密度

1.04 g/mL at 25 °C (lit.)

SMILES 字串

CCOC(=O)C1CCCCCCC1=O

InChI

1S/C11H18O3/c1-2-14-11(13)9-7-5-3-4-6-8-10(9)12/h9H,2-8H2,1H3

InChI 密鑰

OJCDCHCBNASPBS-UHFFFAOYSA-N

一般說明

Ethyl 2-oxo-1-cyclooctanecarboxylate (2-carbethoxycyclooctanone) is a β-keto ester. It undergoes Michael addition with 3-buten-2-one (methyl vinyl ketone, MVK) in the presence of potassium bis(1,2-benzenediolato)phenylsilicate to afford the corresponding 1,4-adduct. It can be synthesized from cycloheptanone. Its boiling point, density and refractive index have been determined.

應用

Ethyl 2-oxo-1-cyclooctanecarboxylate (2-carbethoxycyclooctanone) may be used in the synthesis of 2-carbethoxy-2-cyclooctenone.

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Activated cyclooctenones are effective dienophiles.
Liu HJ, et al.
Canadian Journal of Chemistry, 75(6), 899-912 (1997)
Pentacoordinate Organosilicate-Catalyzed Michael Addition of ?-Keto Esters to 3-Buten-2-one.
Tateiwa J-U and Hosomi A.
European Journal of Organic Chemistry, 2001(8), 1445-1448 (2001)
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 336-336 (2015)

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