307475
Pyridine hydrobromide
98%
Sinónimos:
Pyridinium bromide
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About This Item
Fórmula empírica (notación de Hill):
C5H5N · HBr
Número de CAS:
Peso molecular:
160.01
Beilstein/REAXYS Number:
3615336
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
solid
assay:
98%
Productos recomendados
Quality Level
assay
98%
form
solid
mp
200 °C (dec.) (lit.)
SMILES string
Br[H].c1ccncc1
InChI
1S/C5H5N.BrH/c1-2-4-6-5-3-1;/h1-5H;1H
InChI key
BBFCIBZLAVOLCF-UHFFFAOYSA-N
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Application
Pyridine hydrobromide may be used in chemical synthesis studies.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Combination of pyridine, antipyrine and indole in a single molecule (L2) allows selective recognition of Fe3+ colorimetrically in CH3CN. The structure of L2 is confirmed from single crystal X-ray diffraction analysis. The probe displays two different visible bands at 541nm
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The reaction of 2,2'-bipyridine (bpy) with monomeric chromium(II) precursors was used to prepare the S = 1 complexes Cr(tBu-acac)2(bpy) (1) and (η(5)-Cp)(η(1)-Cp)Cr(bpy) (3), as well as the S = 2 compound Cr[N(SiMe3)2]2(bpy) (4). The crystallographically determined bond lengths indicate that
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A pentafluorophenyl (–C6F5) substituted 3-pyridyl urea, L(1), is explored extensively to demonstrate SO4(2-) binding exclusively via second sphere coordination in the cavity of a 1D polymeric self-assembly of L(1), selectively assisted by Cu2+. A single crystal X-ray diffraction study depicts
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A series of bis(oxazolidine)pyridine ligands (the PyBodines) were newly designed and synthesized for the development of a highly efficient, tailor-made catalyst for the [3+2] cycloaddition of azomethine imines with propiolates. The PyBodine(l-Ala)-Cu(OAc)2 catalyst was selected on the basis of solid-phase
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