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Merck
CN

62760

Sigma-Aldrich

2,6-二甲基吡啶

purum, ≥96.0% (GC)

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别名:
2,6-卢剔啶
经验公式(希尔记法):
C7H9N
CAS号:
分子量:
107.15
Beilstein:
105690
EC 号:
MDL编号:
UNSPSC代码:
12352000

等级

purum

检测方案

≥96.0% (GC)

折射率

n20/D 1.497 (lit.)
n20/D 1.498

bp

143-145 °C (lit.)

mp

−6 °C (lit.)

密度

0.92 g/mL at 25 °C (lit.)

SMILES字符串

Cc1cccc(C)n1

InChI

1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3

InChI key

OISVCGZHLKNMSJ-UHFFFAOYSA-N

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象形图

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警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

WGK

WGK 3

闪点(°F)

91.4 °F

闪点(°C)

33 °C

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Wensheng Yu et al.
Organic letters, 6(19), 3217-3219 (2004-09-10)
[reaction: see text] Oxidative cleavage of olefins by OsO(4)-NaIO(4) sometimes suffers from low yields due to the formation of side products. It is found that the addition of 2,6-lutidine can suppress the side reactions and dramatically improve the yield of
Kathryn A White et al.
Journal of colloid and interface science, 359(1), 126-135 (2011-04-22)
Using a system of modified silica particles and mixtures of water and 2,6-lutidine to form particle-stabilized emulsions, we show that subtle alterations to the hydration of the particle surface can cause major shifts in emulsion structure. We use fluorescence confocal
Qingnan Liu et al.
The journal of physical chemistry. A, 113(16), 4387-4396 (2009-03-24)
Collision rates and energy transfer distributions are reported for HOD with highly vibrationally excited 2-methylpyridine (2-picoline, E = 38 310 cm(-1)) and 2,6-dimethylpyridine (2,6-lutidine, E = 38 700 cm(-1)). High resolution transient IR absorption is used measured to complete product
Cyrille Costentin et al.
Journal of the American Chemical Society, 132(29), 10142-10147 (2010-07-06)
The effect of base pairing by cytosine on the electrochemical oxidation of guanine is examined by means of cyclic voltammetry on carefully purified reactants in a solvent, CHCl(3), which strongly favors the formation of an H-bonded pair. The thermodynamics and
Elena Arceo et al.
Nature chemistry, 5(9), 750-756 (2013-08-24)
Asymmetric catalytic variants of sunlight-driven photochemical processes hold extraordinary potential for the sustainable preparation of chiral molecules. However, the involvement of short-lived electronically excited states inherent to any photochemical reaction makes it challenging for a chiral catalyst to dictate the

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