B80429
4-溴吡啶 盐酸盐
99%
别名:
4-溴吡啶单盐酸盐, 4-溴吡啶盐酸盐
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关于此项目
经验公式（希尔记法）:
C5H4BrN · HCl
化学文摘社编号:
分子量:
194.46
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
243-128-4
Beilstein/REAXYS Number:
3680350
MDL number:
产品名称
4-溴吡啶 盐酸盐, 99%
InChI
1S/C5H4BrN.ClH/c6-5-1-3-7-4-2-5;/h1-4H;1H
InChI key
MPZMVUQGXAOJIK-UHFFFAOYSA-N
SMILES string
Cl[H].Brc1ccncc1
assay
99%
form
crystals
mp
270 °C (dec.) (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Ekaterina A Dolgopolova et al.
Journal of the American Chemical Society, 141(13), 5350-5358 (2019-03-07)
Electronic structure modulation of metal-organic frameworks (MOFs) through the connection of linker "wires" as a function of an external stimulus is reported for the first time. The established correlation between MOF electronic properties and photoisomerization kinetics as well as changes
Thomas M Kohl et al.
Molecules (Basel, Switzerland), 20(10), 17860-17871 (2015-10-02)
Significant process intensification of the amination reactions of aryl halides and esters has been demonstrated using continuous flow processing. Using this technology traditionally difficult amination reactions have been performed safely at elevated temperatures. These reactions were successfully conducted on laboratory
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