推荐产品
质量水平
产品线
ReagentPlus®
检测方案
99%
形式
liquid
折射率
n20/D 1.498 (lit.)
bp
171-172 °C (lit.)
mp
−43 °C (lit.)
密度
0.917 g/mL at 25 °C (lit.)
SMILES字符串
Cc1cc(C)nc(C)c1
InChI
1S/C8H11N/c1-6-4-7(2)9-8(3)5-6/h4-5H,1-3H3
InChI key
BWZVCCNYKMEVEX-UHFFFAOYSA-N
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一般描述
2,4,6-三甲基吡啶是一种吡啶衍生物。它具有7.4的pK。该产物可与环戊烷溶液中的三氟碘甲烷反应生成1:1的络合物。可通过NMR(核磁共振)光谱对该络合物进行研究。通过向其中加入四氧化锇溶液来制备可力丁缓冲的四氧化锇溶液。这些溶液已被用作电子显微镜研究的固定剂。
2,4,6-三甲基吡啶可用高锰酸钾氧化形成2,4,6-吡啶三羧酸。
2,4,6-三甲基吡啶可用高锰酸钾氧化形成2,4,6-吡啶三羧酸。
受阻的基底。
应用
2,4,6-三甲基吡啶(可力丁,s-可力丁,2,4,6-可力丁)已被用于制备带有低分子量N-酰基的N-酰基氨基香豆素的文库。
可用于通过无水碘化锂裂解位阻酯的有用溶剂。
用作电子显微镜的组织固定剂。
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语:
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Synthesis, structure, photoluminescence and magnetic properties of new 3-D lanthanide-pyridine-2, 4, 6-tricarboxylate frameworks
CrystEngComm, 10(11), 1645-1652 (2008)
The journal of physical chemistry. A, 110(3), 1128-1133 (2006-01-20)
Ab initio EOM-CCSD calculations have been performed on 3:1 FH:NH3 complexes at their own optimized MP2/6-31+G(d,p) geometries and at the optimized geometries in the hydrogen-bonding regions of corresponding 3:1 FH:collidine complexes. The isolated gas-phase equilibrium 3:1 FH:NH3 complex has an
Histochemistry, 89(3), 301-306 (1988-01-01)
In previous work of our laboratory it was demonstrated that collidine (2,4,6-trimethylpyridine) abolishes the core osmiophilia and chromaffin reaction from rat pinal gland and vas deferens nerves. This abolition was apparent when tissues were briefly incubated in collidine or when
Magnetic resonance in chemistry : MRC, 48(6), 417-426 (2010-05-18)
(1)H, (13)C and (15)N NMR studies of gold(III), palladium(II) and platinum(II) chloride complexes with dimethylpyridines (lutidines: 2,3-lutidine, 2,3lut; 2,4-lutidine, 2,4lut; 3,5-lutidine, 3,5lut; 2,6-lutidine, 2,6lut) and 2,4,6-trimethylpyridine (2,4,6-collidine, 2,4,6col) having general formulae [AuLCl(3)], trans-[PdL(2)Cl(2)] and trans-/cis-[PtL(2)Cl(2)] were performed and the respective
Chemistry, an Asian journal, 7(2), 367-373 (2011-12-14)
Mild substitution reactions of acetals with carbon nucleophiles via the pyridinium-type salts generated by the treatment of acetals with TESOTf-2,4,6-collidine or 2,2'-bipyridyl have been developed. Various carbon nucleophiles, such as organocuprates, silyl enol ethers, enamines, etc., reacted with the pyridinium-type
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