推薦產品
品質等級
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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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
從最近期的版本中選擇一個：
分析證明 (COA)
Lot/Batch Number
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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
Journal of Organometallic Chemistry, 447, 299-299 (1993)
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)
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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