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307475

Sigma-Aldrich

Pyridine hydrobromide

98%

Sinónimos:

Pyridinium bromide

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About This Item

Fórmula empírica (notación de Hill):
C5H5N · HBr
Número de CAS:
18820-82-1
Peso molecular:
160.01
Beilstein/REAXYS Number:
3615336
EC Number:
242-600-7
MDL number:
MFCD00012801
UNSPSC Code:
12352100
PubChem Substance ID:
24858596
NACRES:
NA.22

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.

pictograms

Exclamation mark
GHS07

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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Sabyasachi Ta et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 173, 196-200 (2016-09-24)
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
Harry Adams et al.
Journal of the American Chemical Society, 135(5), 1853-1863 (2013-01-31)
The association constants for a family of 96 closely related zinc porphyrin-pyridine ligand complexes have been measured in two different solvents, toluene and 1,1,2,2-tetrachloroethane (TCE). The zinc porphyrin receptors are equipped with phenol side arms, which can form intramolecular H-bonds
Jipan Yu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(13), 4271-4277 (2013-02-13)
Efficient copper-catalyzed aerobic oxidative C-H and C-C functionalization of 1-[2-(arylamino)aryl]ethanones leading to acridones has been developed. The procedure involves cleavage of aromatic C-H and acetyl C-C bonds with intramolecular formation of a diarylketone bond. The protocol uses inexpensive Cu(O2CCF3)2 as
Yuya Kodama et al.
Journal of medicinal chemistry, 56(22), 9342-9350 (2013-11-01)
In this study, we developed an assignment-free approach for rapid identification of ligand-binding sites in target proteins by using NMR. With a sophisticated cell-free stable isotope-labeling procedure that introduces (15)N- or (13)C-labels to specific atoms of target proteins, this approach
V Subbaramaiah et al.
Journal of hazardous materials, 248-249, 355-363 (2013-02-19)
Cerium supported SBA-15 (Ce/SBA-15) was synthesized by two-step synthesis method in acidic medium. It was further characterized by various characterization techniques such as X-ray diffraction, field-emission scanning electron microscopy, Fourier transform infrared spectroscopy and N2 adsorption-desorption pore size distribution analysis.
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