Amines

2-Amino-7-nitrofluorene is a molecule that has two nitro groups and one amino group. 2-Amino-7-nitrofluorene is a solute that has a dipole moment and can form hydrogen bonds with other molecules. The viscosity of 2-amino-7-nitrofluorene depends on the concentration of the solution, which can be calculated using simulations. The optical properties of 2-amino-7-nitrofluorene are dependent on its molecular structure. Phenyl groups in the molecule absorb light at wavelengths greater than 350 nanometers and contribute to its color (yellow). Photophysical reactions include electron transfer, which occurs when the electrons in one molecule are excited by energy from another source (e.g., UV radiation) and then jump to another molecule, transferring their energy in the process. Transfer reactions occur when one reactant transfers its atoms or molecules to another reactant, resulting in

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5-Amino-1-phenylpyrazole is a heterocyclic amine with insecticidal activity. It has been shown to be effective against larvae of the cabbage butterfly, Pieris rapae. The mode of action may be due to inhibition of cholinesterase activity in the insect's nervous system. 5-Amino-1-phenylpyrazole also has fluorescence properties and can be used as a fluorescent probe for detecting reaction mechanism.

2-[(7-Fluoro-9-Oxoxanthen-2-Yl)Sulfonyl-Methylamino]Acetic Acid is a potent inhibitor of the enzyme dehydrogenase. It has been shown to reduce serum glucose levels in animal studies and shift the profile of albumin, as well as reducing proteinuria. 2-[(7-Fluoro-9-Oxoxanthen-2-Yl)Sulfonyl-Methylamino]Acetic Acid may be an effective treatment for diabetes mellitus, especially in those with renal failure.

Applications 2,3-Dimethyl-2H-indazol-6-ylamine is a reagent used in the synthesis of Pazopanib derivatives as antitumor agents. References Jia, Y., et al.: Chem. Biol. Drug Design, 83, 306 (2014)

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