19798-80-2
19798-80-2
Chemical Structure
2-Amino-4-chloropyridine
- CAS No.: 19798-80-2
- Formula:C5H5ClN2
- Molecular Weight:128.56
IUPAC Name: 4-chloropyridin-2-amine
InChIKey: RQMWVVBHJMUJNZ-UHFFFAOYSA-N
SMILES: NC1=NC=CC(Cl)=C1
Biological Activity: 2-Amino-4-chloropyridine is a key intermediate. 2-Amino-4-chloropyridine derivatives exhibit antibacterial activity against Gram-positive bacteria, Gram-negative bacteria, and fungi[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-Amino-4-chloropyridine | 98.90% | 2-Amino-4-chloropyridine is a key intermediate. 2-Amino-4-chloropyridine derivatives exhibit antibacterial activity against Gram-positive bacteria, Gram-negative bacteria, and fungi. | ||||||||||||||||||||
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4-Amino-2-chloropyrimidine | 99.77% | 4-Amino-2-chloropyrimidine is a pyrimidine derivative. 4-Amino-2-chloropyrimidine is a competitive inhibitor for AChE (Ki = 0.18 μM) and BChE (Ki = 1.324 μM). 4-Amino-2-chloropyrimidine fits in the binding pocket of 4BDS. 4-Amino-2-chloropyrimidine has high inhibitory activity on GST enzyme activity (IC50 = 0.037 μM, Ki = 0.047 μM) in vitro. | ||||||||||||||||||||
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2-Chloro-4-iodopyridine | 99.97% | 2-Chloro-4-iodopyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-Amino-4-chloropyridine | 98.46% | 3-Amino-4-chloropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2-Amino-4-bromopyridine | 99.98% | 2-Amino-4-bromopyridine (4-Bromopyridine-2-amine) is an important intermediate, which can be used for the synthesis of other active compounds. | ||||||||||||||||||||
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2-Bromo-4-chloropyridine | 98.96% | 2-Bromo-4-chloropyridine is a halogenated pyridine derivative that serves as a synthetic intermediate. 2-Bromo-4-chloropyridine undergoes Suzuki-Miyaura coupling with 4-tert-butylphenylboronic acid (HY-W007389). 2-Bromo-4-chloropyridine facilitates the construction of compounds with broad-spectrum antibacterial activity. | ||||||||||||||||||||
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Aminopicoline (Standard) | ≥98% | Aminopicoline (Standard) is the analytical standard of Aminopicoline. Aminopicoline (Ascensil) is a potent and non-selective inhibitor of nitric oxide synthase (NOS) isoenzymes (iNOS, nNOS, eNOS). Aminopicoline competes with arginine at the substrate-binding site of nitric oxide synthase, reduces cellular nitric oxide production, inhibits the elevation of plasma nitrate, increases mean arterial pressure at high doses, and also serves as a basis for radiolabeled ligands to localize nitric oxide synthase binding sites. Aminopicoline can be used in the research of diseases associated with septic shock, joint inflammation, intestinal inflammation, and CNS inflammation。 | ||||||||||||||||||||
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2-Amino-4-fluoropyridine | 99.97% | 2-Amino-4-fluoropyridine (4-Fluoropyridin-2-amine) is an intermediate. 2-Amino-4-fluoropyridine can be used in research on the synthesis of PKCζ inhibitors. | ||||||||||||||||||||
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6-Chloropyridin-3-amine | 99.94% | 6-Chloropyridin-3-amine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2-Chloropyridin-3-amine | 99.95% | 2-Chloropyridin-3-amine is a heterocyclic amine that serves as a pharmaceutical intermediate for the synthesis of dihydroorotate dehydrogenase (DHODH) inhibitors. | ||||||||||||||||||||
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2-Amino-5-chloropyridine (Standard) | ≥98% | 2-Amino-5-chloropyridine (Standard) is the analytical standard of 2-Amino-5-chloropyridine. This product is intended for research and analytical applications. | ||||||||||||||||||||
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