Home > Compound List > Product Information
4,4′-Azopyridine_Molecular_structure_CAS_2632-99-7)
Click picture or here to close

4,4′-Azopyridine

Catalog No. 705055 Name Sigma Aldrich
CAS Number 2632-99-7 Website http://www.sigmaaldrich.com
M. F. C10H8N4 Telephone 1-800-521-8956
M. W. 184.19732 Fax
Purity Email
Storage Chembase ID: 141786

SYNONYMS

Title
4,4′-偶氮吡啶
IUPAC name
4-[2-(pyridin-4-yl)diazen-1-yl]pyridine
IUPAC Traditional name
4-[2-(pyridin-4-yl)diazen-1-yl]pyridine
Synonyms
Azobis(4-pyridine)

DATABASE IDS

MDL Number MFCD00129061
CAS Number 2632-99-7

PROPERTIES

Empirical Formula (Hill Notation) C10H8N4
Melting Point 96-101 °C
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H315-H319-H335
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P261-P301 + P310-P305 + P351 + P338
RID/ADR UN 2811 6.1/PG 3
Risk Statements 22-36/37/38
Safety Statements 26-36/37
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reactant for preparation of:
• Flexible porous coordination polymers constructed from 1,2-bis(4-pyridyl)hydrazine via solvothermal in situ reduction reaction1
• Metal-organic frameworks based on transition-metal carboxylate clusters as secondary building units2
• Heteroaromatic azo compounds under Mitsunobu conditions3
• MnII, CoII, and ZnII coordination polymers4
• Low-dimensional and porous coordination compounds capable of supramolecular aromatic interactions5Reagent in:
• Facile Mitsunobu esterification reactions6
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant for preparation of:
• Flexible porous coordination polymers constructed from 1,2-bis(4-pyridyl)hydrazine via solvothermal in situ reduction reaction1
• Metal-organic frameworks based on transition-metal carboxylate clusters as secondary building units2
• Heteroaromatic azo compounds under Mitsunobu conditions3
• MnII, CoII, and ZnII coordination polymers4
• Low-dimensional and porous coordination compounds capable of supramolecular aromatic interactions5Reagent in:
• Facile Mitsunobu esterification reactions6

REFERENCES