5469-69-2
Chemical Structure
3-Amino-6-chloropyridazine
- CAS No.: 5469-69-2
- Formula:C4H4ClN3
- Molecular Weight:129.55
IUPAC Name: 6-chloropyridazin-3-amine
InChIKey: DTXVKPOKPFWSFF-UHFFFAOYSA-N
SMILES: NC1=NN=C(Cl)C=C1
Biological Activity: 3-Amino-6-chloropyridazine is a nitrogen-containing heterocyclic organic compound belonging to the pyridazine derivatives. 3-Amino-6-chloropyridazine has the basicity of amino groups and the nucleophilic substitution activity of chlorine atoms. 3-Amino-6-chloropyridazine can serve as an important intermediate for synthesizing some active compounds[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-Amino-6-chloropyridazine | 98.0% | 3-Amino-6-chloropyridazine is a nitrogen-containing heterocyclic organic compound belonging to the pyridazine derivatives. 3-Amino-6-chloropyridazine has the basicity of amino groups and the nucleophilic substitution activity of chlorine atoms. 3-Amino-6-chloropyridazine can serve as an important intermediate for synthesizing some active compounds. | ||||||||||||||||||||
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2-Amino-4-chloropyrimidine | 2-Amino-4-chloropyrimidine is an aminopyrimidine derivative. | |||||||||||||||||||||
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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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3,6-Dibromopyridazine | 99.92% | 3,6-Dibromopyridazine is a brominated pyridazine heterocycle used as a synthetic precursor. 3,6-Dibromopyridazine is an important intermediate in organic synthesis. 3,6-Dibromopyridazine is mainly used in pharmaceutical intermediates, organic synthesis, and organic solvents, and can also be used in dye production, pesticide production, and perfume manufacturing. | ||||||||||||||||||||
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2-Amino-6-chloropyrazine | 99.87% | 2-Amino-6-chloropyrazine 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-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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3-Chloro-6-methoxypyridazine | 3-Chloro-6-methoxypyridazine 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-Chloro-6-methylpyridazine | 98.05% | 3-Chloro-6-methylpyridazine is a substituted pyridazine derivative containing an electron-withdrawing chlorine atom and an electron-donating methyl group. Pyridazine compounds generally possess pharmacological activities such as antibacterial and anti-inflammatory properties. 3-Chloro-6-methylpyridazine can serve as an organic ligand for constructing organic-inorganic hybrid chloroantimonate materials with semiconducting behavior. 3-Chloro-6-methylpyridazine can be used in studies related to optoelectronic devices, photodetectors, and photocatalysis. | ||||||||||||||||||||
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2,6-Dichloro-3-pyridinamine | 99.63% | 2,6-Dichloro-3-pyridinamine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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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-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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References
- [1]. HORIE T, et al. Studies on pyridazine derivatives. I. Synthesis and antimicrobial activity of 6-substituted 3-aminopyridazine and its sulfonamido derivatives. Chem Pharm Bull (Tokyo). 1962 Jul;10:580-91. [Content Brief]
- [2]. Hu M M, et al. 3-Amino-6-chloropyridazinium chloride. Structure Reports, 2007, 63(11): o4292-o4292.