705055
4,4′-Azopyridine
Synonym(s):
Azobis(4-pyridine)
About This Item
form
solid
mp
96-101 °C
SMILES string
c1cc(ccn1)N=Nc2ccncc2
InChI
1S/C10H8N4/c1-5-11-6-2-9(1)13-14-10-3-7-12-8-4-10/h1-8H
InChI key
XUPMSLUFFIXCDA-UHFFFAOYSA-N
General description
Application
- To prepare porous coordination polymers (PCPs) by reacting with Zn(NO3)2 and 1,4-benzenedicarboxylic acid.
- As a reagent for the conversion of aliphatic alcohols into disulfides under Mitsunobu conditions.
- To prepare 4,4′-azopyridine-bridged binuclear zinc(II) complexes.
- Flexible porous coordination polymers constructed from 1,2-bis(4-pyridyl)hydrazine via solvothermal in situ reduction reaction
- Metal-organic frameworks based on transition-metal carboxylate clusters as secondary building units
- Heteroaromatic azo compounds under Mitsunobu conditions
- MnII, CoII, and ZnII coordination polymers
- Low-dimensional and porous coordination compounds capable of supramolecular aromatic interactions
Reagent in:
- Facile Mitsunobu esterification reactions
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service