125857
2,3-二氨基吡啶
95%
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关于此项目
经验公式（希尔记法）:
C5H7N3
化学文摘社编号:
分子量:
109.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-200-9
Beilstein/REAXYS Number:
109869
MDL number:
产品名称
2,3-二氨基吡啶, 95%
InChI key
ZZYXNRREDYWPLN-UHFFFAOYSA-N
InChI
1S/C5H7N3/c6-4-2-1-3-8-5(4)7/h1-3H,6H2,(H2,7,8)
SMILES string
Nc1cccnc1N
assay
95%
form
powder
mp
110-115 °C (lit.)
solubility
H2O: soluble 50 mg/mL, opaque (brown to very dark brown)
Quality Level
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Application
2,3-二氨基吡啶被用于合成2,3-二氨基吡啶-4-羟基苯甲酸酯。其可作为内标，通过毛细管电泳分析具有不同末端官能度的聚（胺基胺）树状聚合物。其可作为试剂，用于合成咪唑并吡啶 和有机金属配合物。
General description
2,3-二氨基吡啶可与水杨醛形成双缩合席夫碱。它可与四氯-p-苯醌和四氰基乙烯形成电荷转移络合物。
signalword
Warning
hcodes
Hazard Classifications
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, Faceshields, Gloves
Hoong-Kun Fun et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 7), o1496-o1497 (2009-01-01)
In the title compound, C(5)H(8)N(3) (+)·C(7)H(5)O(3) (-), the pyridine N atom is protonated. In the 4-hydroxy-benzoate anion, the carboxyl-ate group is twisted slightly out of the benzene ring plane by an angle of 3.77 (5)°. The protonated N atom and one
Synthesis and anti-bacterial/catalytic properties of Schiff bases and Schiff base metal complexes derived from 2, 3-diaminopyridine.
Jeewoth T, et al.
Synth. React. Inorg. Met.-Org. Chem. , 30(6), 1023-1038 (2000)
Journal of Organometallic Chemistry, 447, 299-299 (1993)
Synthesis and Spectroscopic Studies of the Charge-Transfer Complexes of 2, 3-Diaminopyridine and p-Electron Acceptors.
Alqaradawi SY and Nour EM.
Spectroscopy Letters, 37(4), 337-345 (2004)
W J Coates et al.
Journal of medicinal chemistry, 36(10), 1387-1392 (1993-05-14)
The synthesis and phosphodiesterase (PDE) inhibitory profile of a series of imidazopyridines, including sulmazole and isomazole, on separated PDE isoenzymes are described. The results show that both sulmazole and isomazole are weak inhibitors of PDE III, and their inotropic activity
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