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Key Documents

469890

Sigma-Aldrich

3-甲氧基吡啶

97%

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About This Item

經驗公式(希爾表示法):
C6H7NO
CAS號碼:
分子量::
109.13
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 1.518 (lit.)

bp

65 °C/15 mmHg (lit.)

密度

1.083 g/mL at 25 °C (lit.)

SMILES 字串

COc1cccnc1

InChI

1S/C6H7NO/c1-8-6-3-2-4-7-5-6/h2-5H,1H3

InChI 密鑰

UMJSCPRVCHMLSP-UHFFFAOYSA-N

一般說明

3-Methoxypyridine is a substituted pyridine. Kinetics of the oxidation of 3-methoxypyridine mediated by sulphate radicals has been investigated by flash photolysis of peroxodisulphate, S2O82-. Ortho lithiation of 3-methoxypyridine has been studied using mesityllithium as the metalating base.

應用

3-Methoxypyridine may be employed as a catalyst for the addition reaction of various 1,2-acyclic diones to activated acetylenic esters.

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)

159.8 °F - closed cup

閃點(°C)

71 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Abhilash N Pillai et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(19), 5851-5860 (2008-05-10)
A systematic study of the addition of various 1,2-acyclic diones to activated acetylenic esters catalyzed by pyridine under mild conditions is described. This reaction provides a new protocol for the stereoselective synthesis of 1,2-diaroyl maleates. The exclusive formation of the
María L Dell'arciprete et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 8(17), 2498-2505 (2007-10-25)
The kinetics of the oxidation of pyridine, 3-chloropyridine, 3-cyanopyridine, 3-methoxypyridine and 3-methylpyridine mediated by SO4 (<M->) radicals are studied by flash photolysis of peroxodisulphate, S2O8(2-), at pH 2.5 and 9. The absolute rate constants for the reactions of both, the
Ortho lithiation of 2-, 3-, and 4-methoxypyridines.
Comins DL and LaMunyon DH.
Tetrahedron Letters, 29(7), 773-776 (1988)

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