429112
2-溴-6-甲基吡啶
98%
别名:
2-溴-6-甲基吡啶, 2-甲基-6-溴吡啶, 6-溴-2-甲基吡啶, 6-甲基-2-溴吡啶
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关于此项目
经验公式（希尔记法）:
C6H6BrN
化学文摘社编号:
分子量:
172.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-173-4
MDL number:
产品名称
2-溴-6-甲基吡啶, 98%
InChI key
SOHDPICLICFSOP-UHFFFAOYSA-N
InChI
1S/C6H6BrN/c1-5-3-2-4-6(7)8-5/h2-4H,1H3
SMILES string
Cc1cccc(Br)n1
assay
98%
form
liquid
refractive index
n20/D 1.562 (lit.)
bp
102-103 °C/20 mmHg (lit.)
density
1.512 g/mL at 25 °C (lit.)
functional group
bromo
Quality Level
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Application
2-溴-6-甲基吡啶可用于以下合成：
- 6,6′-二甲基-2,2′-联吡啶
- 6-甲基-2-吡啶基-2-吡啶基甲酮
- 2-甲基-6-（三甲基硅基）-吡啶
- N , N '-双-（6-甲基吡啶-2-基）-(1 R ,2 R )-1,2-二氨基环己烷 (cydiampy)
- 2-甲基-6-吡啶
- 2-（6-甲基吡啶-2-基）丙-2-醇
- 双 [（2-溴-6-甲基吡啶）六氟硅酸盐] 一水合物
General description
2-溴-6-甲基吡啶是溴吡啶衍生物。2-氯-6-甲基吡啶与溴三甲基硅烷加热时形成。已报道通过各种方法合成这种物质。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
206.6 °F - closed cup
flash_point_c
97 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Nickel complexes with new bidentate P,N phosphinitooxazoline and-pyridine ligands: Application for the catalytic oligomerization of ethylene.
Speiser F, et al.
Inorganic Chemistry, 43(5), 1649-1658 (2004)
Catalytic Asymmetric Synthesis of Bis-armed Aromatic Amino Acid Derivatives. Problems Related to the Synthesis of Enantiomerically Pure Bis-methyl Ester of the (S,S)-Pyridine-2,6-diyl Bis-alanine.
Basu B and FrejdT T.
Acta Chemica Scandinavica, 50, 316-322 (1996)
Block copolymers with bipyridine containing segments: Synthesis and self-organization by Cu (I) complexation.
2Eisenbach CD, et al.
Macromolecular Chemistry and Physics, 196(4), 1077-1091 (1995)
3-(2-Pyridyl)-[1,2,3] triazolo [1,5-a] pyridines. An experimental and theoretical (DFT) study of the ring-chain isomerization.
Abarca B, et al.
Organic & Biomolecular Chemistry, 3(21), 3905-3910 (2005)
Preparation, structure and properties of pyridinium/bipyridinium hexafluorosilicates.
Gelmboldt VO, et al.
Journal of Fluorine Chemistry, 160, 57-63 (2014)
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