6980-08-1 | 2-Amino-4-chloro-3-nitropyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$20.00	$14.00
5g	96%	in stock	$63.00	$44.00
10g	95%	in stock	$73.00	$51.00
25g	95%	in stock	$179.00	$126.00

Description

• Catalog Number: AH15697
• Chemical Name: 2-Amino-4-chloro-3-nitropyridine
• CAS Number: 6980-08-1
• Molecular Formula: C5H4ClN3O2
• Molecular Weight: 173.5572
• MDL Number: MFCD04116097
• SMILES: [O-][N+](=O)c1c(Cl)ccnc1N

Computed Properties

• Complexity: 160
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.5

Upstream Synthesis Route

4-Chloro-3-nitropyridin-2-amine, also known as $name$, serves as a crucial building block in the field of chemical synthesis. This compound is often utilized for its remarkable reactivity and versatility in organic reactions.In chemical synthesis, $name$ plays a key role as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and functional groups make it a valuable starting material for the synthesis of complex molecules with specific biological or industrial applications.One common application of 4-Chloro-3-nitropyridin-2-amine is in the formation of heterocyclic compounds, which are essential in the development of new drug candidates and advanced materials. By utilizing this compound as a precursor, chemists can introduce specific functional groups and manipulate the molecular structure to design molecules with desired properties.Additionally, the presence of the chlorine and nitro groups in 4-Chloro-3-nitropyridin-2-amine enables selective transformations through various chemical reactions such as nucleophilic substitution, reduction, and metal-catalyzed coupling reactions. This versatility allows chemists to tailor the molecular properties of the final product for specific applications in the pharmaceutical and agrochemical industries.Overall, the strategic use of 4-Chloro-3-nitropyridin-2-amine in chemical synthesis offers a pathway to access diverse chemical space and facilitate the discovery and development of novel compounds with potential therapeutic, agricultural, or industrial significance.