Weight | 125.135 g/mol |
---|---|
Formula | C4H7N5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,4,6-Triaminopyrimidine (1004-38-2)
Score:
#2245 in Physics
,
#2827 in Biochemistry
,
#5284 in Biology
,
#6945 in Chemistry
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- Zeolite-filled polyimide membrane containing 2,4,6-triaminopyrimidine (Journal of Membrane Science, 2001)
- Copolymerization with 2,4,6-triaminopyrimidine for the rolling-up the layer structure, tunable electronic properties, and photocatalysis of g-C3N4. (ACS Applied Materials & Interfaces, 2015)
- On the cross-reactivity of amiloride and 2,4,6 Triaminopyrimidine (TAP) for the cellular entry and tight junctional cation permeation pathways in epithelia (The Journal of Membrane Biology, 1979)
- Molecular recognition-induced function and competitive replacement by hydrogen-bonding interactions: amphiphilic barbituric acid derivatives, 2,4,6-triaminopyrimidine, and related structures at the air-water interface. (Langmuir, 1999)
- Condensed pyrimidine systems. XXIV. The condensation of 2,4,6-triaminopyrimidine with malondialdehyde derivatives (Journal of Medicinal Chemistry, 1968)
- Barbituric acid/2,4,6-triaminopyrimidine aggregates in water and their competitive interaction with a monolayer of barbituric acid lipids at the gas-water interface (Angewandte Chemie, 1995)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(N=C(N=C1N)N)N
-
InChIKeyJTTIOYHBNXDJOD-UHFFFAOYSA-N
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Similar Compounds
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cytosine
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