质量水平
方案
99%
表单
solid
mp
73-78 °C (lit.)
官能团
chloro
SMILES字符串
ClCc1cccc(CCl)n1
InChI
1S/C7H7Cl2N/c8-4-6-2-1-3-7(5-9)10-6/h1-3H,4-5H2
InChI key
IWQNFYRJSVJWQA-UHFFFAOYSA-N
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一般描述
2,6-双（氯甲基）吡啶是用于合成多种吡啶衍生物的杂环结构单元。它通过 N 原子与金属离子配位形成配合物。溴甲基臂的构象灵活性使其成为生成大环的理想选择。2,6-双（氯甲基）吡啶晶体为单斜晶，空间群为 P21/c。已有研究报道了它的合成。2,6-双（氯甲基）吡啶（BCMP）的 FT-IR 和 Ft-拉曼光谱分别在4000-400cm-1 和 3500-100cm-1 区域进行了记录。
应用
2,6-双（氯甲基）吡啶可用于以下研究中：
- 合成用于 Hg2+ 的敏感荧光化学传感器，该传感器由两个氨基萘二甲酰亚胺荧光团和 2,6-双（氨基甲基）吡啶的受体组成。
- 卡宾钳配体的制备，用于制备钯钳卡宾配合物。
- 合成 2-（二叔丁基膦基甲基）-6-二乙氨基甲基）吡啶，一种 PNN 配体。
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
V Balachandran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 1023-1032 (2012-08-29)
The FT-IR and FT-Raman spectra of 2,6-Bis(chloromethyl)pyridine (BCMP) have been recorded in the regions 4000-400 cm(-1) and 3500-100 cm(-1), respectively. The total energy calculations of BCMP were tried for the possible rotational isomers. The molecular structure, geometry optimization, vibrational frequencies
Xiangfeng Guo et al.
Journal of the American Chemical Society, 126(8), 2272-2273 (2004-02-26)
A selective and sensitive fluorescent chemosensor for Hg2+, which was composed of two aminonaphthalimide fluorophores and a receptor of 2,6-bis(aminomethyl)pyridine, was synthesized through the reaction of 2,6-bis(chloromethyl)pyridine and N-[2-(2-hydroxyethoxy)ethyl]-4-piperazino-1,8-naphthalimide. The chemosensor showed an about 17-fold increase in fluorescence quantum yield
Tridentate carbene CCC and CNC pincer palladium (II) complexes: structure, fluxionality, and catalytic activity.
Grundemann S, et al.
Organometallics, 20(25), 5485-5488 (2001)
Iron (II) complexes based on electron-rich, bulky PNN-and PNP-type ligands.
Zhang J, et al.
Inorgorganica Chimica Acta, 359(6), 1955-1960 (2006)
An efficient synthesis of 2,6-bis(chloromethyl)pyridine and a [5.5](2,6) pyridinophane disulfite.
Rezzonico B and Grignon-Dubois M.
J. Chem. Res. Synop., 4, 142-143 (1994)
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