307475
吡啶 氢溴酸盐
98%
别名:
吡啶氢溴酸盐
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关于此项目
经验公式（希尔记法）:
C5H5N · HBr
化学文摘社编号:
分子量:
160.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-600-7
Beilstein/REAXYS Number:
3615336
MDL number:
Assay:
98%
Form:
solid
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
Application
氢溴酸吡啶可用于化学合成研究。
signalword
Warning
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
法规信息
新产品
此项目有
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
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
Prasanta Das et al.
The Journal of chemical physics, 138(5), 054307-054307 (2013-02-15)
With infrared absorption spectra we investigated the reaction between Cl atom and pyridine (C(5)H(5)N) in a para-hydrogen (p-H(2)) matrix. Pyridine and Cl(2) were co-deposited with p-H(2) at 3.2 K; a planar C(5)H(5)N-Cl(2) complex was identified from the observed infrared spectrum
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| 货号 | GTIN |
|---|---|
| 307475-250G | 04061826673539 |