Name | 2,2'-dipyridylamine |
Synonyms | Dipyridylamine 2,2-DIPYRIDYLAMINE 2,2'-DIPYRIDYLAMINE 2,2-IMINODIPYRIDINE 2,2'-dipyridylamine 2,2'-IMINODIPYRIDINE Pyridine, 2,2'-iminodi- n-2-pyridinyl-2-pyridinamine |
CAS | 1202-34-2 |
EINECS | 214-864-3 |
InChI | InChI=1/C10H9N3/c1-3-7-11-9(5-1)13-10-6-2-4-8-12-10/h1-8H,(H,11,12,13) |
Molecular Formula | C10H9N3 |
Molar Mass | 171.2 |
Density | 1.1984 (rough estimate) |
Melting Point | 90-92°C(lit.) |
Boling Point | 222°C50mm Hg(lit.) |
Flash Point | 170°C |
Solubility | Acetonitrile (Slightly), Chloroform (Slightly), Methanol (Slightly) |
Vapor Presure | 0.001mmHg at 25°C |
Appearance | White to yellow powder or crystalline or lumpy |
Color | White to Off-White |
BRN | 127131 |
pKa | 4.79±0.10(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.6550 (estimate) |
MDL | MFCD00006247 |
Use | Metal complex carrier. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
UN IDs | UN 3545 |
WGK Germany | 3 |
RTECS | UR3545000 |
HS Code | 29333990 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Introduction | 2,2'-dipyridinamide is an organic compound, which consists of a pair of 2-pyridinyl (C5H4N) connected to secondary amine composition. It can form a series of coordination complexes. Its conjugate base 2,2 '-bipyridinamide can generate metal atom chains. |
Application | 2,2 ′-dipyridinamide is an organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory organic synthesis process and chemical medicine In the synthesis process, there are reports that it can be used to prepare palladium nanoparticles and palladium nanoparticles. |
Preparation | Tri-tert-butylphosphine, palladium acetate, and sodium tert-butoxide were added to a solution of 2-aminopyridine and 2-bromopyridine in deaerated toluene, and the mixture was heated under reflux for 2 hours. The reaction mixture was cooled to room temperature, diluted with toluene and filtered via diatomite. The filtrate is diluted with water, extracted with toluene, and organic phases are combined, which is evaporated under vacuum. The residue was filtered via silica gel and then re-purified to obtain 2,2 ′-dipyridinamide. |
use | metal complex carrier. |