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化驗
95%
形狀
powder
mp
110-115 °C (lit.)
溶解度
H2O: soluble 50 mg/mL, opaque (brown to very dark brown)
SMILES 字串
Nc1cccnc1N
InChI
1S/C5H7N3/c6-4-2-1-3-8-5(4)7/h1-3H,6H2,(H2,7,8)
InChI 密鑰
ZZYXNRREDYWPLN-UHFFFAOYSA-N
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一般說明
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。
應用
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。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
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)
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 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)
Madhukar Hemamalini et al.
Acta crystallographica. Section E, Structure reports online, 67(Pt 11), o3122-o3122 (2012-01-06)
In the title hydrated mol-ecular salt, C(5)H(8)N(3) (+)·C(7)H(5)O(6)S(-)·H(2)O, the ion pairs and water mol-ecules are connected by N-H⋯O, O-H⋯O and C-H⋯O hydrogen bonds, thereby forming a three-dimensional network. There is an intra-molecular O-H⋯O hydrogen bond in the 3-carb-oxy-4-hy-droxy-benzene-sulfonate anion, which
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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