80866-77-9 | 2-Chloro-6-nitroanisole

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$15.00	$10.00
10g	97%	in stock	$16.00	$12.00
25g	97%	in stock	$34.00	$24.00

Description

• Catalog Number: AC56809
• Chemical Name: 2-Chloro-6-nitroanisole
• CAS Number: 80866-77-9
• Molecular Formula: C7H6ClNO3
• Molecular Weight: 187.5804
• MDL Number: MFCD00065066
• SMILES: COc1c(Cl)cccc1[N+](=O)[O-]

Computed Properties

• Complexity: 171
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 2.4

Upstream Synthesis Route

Application of 2-Chloro-6-nitroanisole in chemical synthesis:2-Chloro-6-nitroanisole holds significant importance in chemical synthesis as a versatile building block. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and advanced materials. Its unique chemical properties and reactivity make it a valuable precursor in the synthesis of diverse organic compounds.In organic synthesis, 2-Chloro-6-nitroanisole can undergo various transformations, such as nucleophilic substitution, aromatic substitution, and reduction reactions, to generate a wide range of functionalized derivatives. These derivatives are crucial for the development of novel drug molecules, herbicides, insecticides, and other specialized chemicals.Furthermore, the presence of both chloro and nitro functional groups in 2-Chloro-6-nitroanisole provides opportunities for further derivatization and modification, allowing chemists to tailor its structure for specific applications. Its ability to participate in cross-coupling reactions and other sophisticated synthetic methodologies enhances its utility in the synthesis of complex molecules.Overall, the use of 2-Chloro-6-nitroanisole as a key synthetic intermediate enables chemists to access a wide array of structurally diverse compounds with valuable properties, contributing to advancements in various fields of chemistry and industry.