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Merck
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文件

425206

Sigma-Aldrich

2-(甲硫基)环己酮

98%

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About This Item

線性公式:
CH3SC6H9(=O)
CAS號碼:
分子量::
144.23
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

化驗

98%

形狀

liquid

折射率

n20/D 1.508 (lit.)

bp

45 °C/10.1 mmHg (lit.)

密度

1.069 g/mL at 25 °C (lit.)

SMILES 字串

CSC1CCCCC1=O

InChI

1S/C7H12OS/c1-9-7-5-3-2-4-6(7)8/h7H,2-5H2,1H3

InChI 密鑰

QFABNUVNDKOIEH-UHFFFAOYSA-N

一般說明

2-(Methylthio)cyclohexanone is a 2-substituted cyclohexanone. The proportion of axial and equatorial conformation has been measured in chloroform by the Eliel method. It suggests that the in chloroform steric effect dominates over polar effect in contributing to the conformational preference. The stereoselectivity of the reduction of 2-(methylthio)cyclohexanone using different hydrides has been studied.

應用

2-(Methylthio)cyclohexanone may be used as a ketone substrate for the synthesis of cyclic nitrones, by reacting with aspergillusol A.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

192.2 °F - closed cup

閃點(°C)

89 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


分析證明 (COA)

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Axial/equatorial proportions for 2-substituted cyclohexanones.
Basso EA, et al.
The Journal of Organic Chemistry, 58(27), 7865-7869 (1993)
Studies on the stereoselectivity of hydride reductions on 2-(methylthio)-and 2-(methylsulfonyl) cyclohexanones.
Carmen CM, et al.
The Journal of Organic Chemistry, 52(16), 3619-3625 (1987)
Nitrone formation in phosphate buffer and aqueous solutions: novel chemistry inspired by a natural product.
Pansanit A, et al.
Tetrahedron Letters, 53(16), 2129-2131 (2012)

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