3964-52-1 | 4-Amino-2-chlorophenol

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$14.00	$10.00
25g	97%	in stock	$40.00	$28.00

Description

• Catalog Number: AB51133
• Chemical Name: 4-Amino-2-chlorophenol
• CAS Number: 3964-52-1
• Molecular Formula: C6H6ClNO
• Molecular Weight: 143.5709
• MDL Number: MFCD00128891
• SMILES: Nc1ccc(c(c1)Cl)O

Computed Properties

• Complexity: 99.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 1.8

Upstream Synthesis Route

4-Amino-2-chlorophenol is a versatile compound widely utilized in chemical synthesis for various applications. In organic synthesis, it serves as a key building block for the preparation of dyes, pharmaceuticals, and agrochemicals. Its unique structure and reactivity make it an essential intermediate in the production of several important compounds.One of the primary applications of 4-Amino-2-chlorophenol is in the manufacture of azo dyes. By reacting with diazonium salts derived from aromatic amines, this compound contributes to the formation of vibrant dyes that are extensively used in textiles, plastics, and other industries. The presence of both amino and chloro groups on the phenolic ring provides opportunities for selective functionalization, allowing for the synthesis of a wide range of dye molecules with diverse properties and colors.Additionally, 4-Amino-2-chlorophenol plays a crucial role in the synthesis of pharmaceutical intermediates. Its incorporation into drug molecules imparts specific therapeutic properties, enabling the development of novel pharmaceuticals with enhanced efficacy and reduced side effects. The structural features of this compound make it a valuable starting material for the synthesis of various biologically active compounds, including antipyretics, analgesics, and antimicrobial agents.Furthermore, in agrochemical synthesis, 4-Amino-2-chlorophenol is utilized for the production of herbicides, insecticides, and fungicides. Its chemical reactivity allows for the modification of its structure to tailor the bioactivity of resulting agrochemical compounds, making them more effective in controlling pests, diseases, and weeds in agricultural settings. By incorporating this compound into the molecular structure of agrochemicals, researchers can design environmentally friendly and sustainable solutions for crop protection.Overall, the versatile nature of 4-Amino-2-chlorophenol makes it an indispensable compound in chemical synthesis, enabling the creation of a wide array of products with applications in various industries, including textiles, pharmaceuticals, and agriculture. Its significance lies in its role as a key intermediate for the synthesis of dyes, pharmaceuticals, and agrochemicals, showcasing its importance in the field of organic chemistry and industrial manufacturing.

Literature

• Rapid determination of aniline metabolites of chlorpropham in potatoes by micellar electrokinetic chromatography using negative-charged mixed micelles and laser-induced fluorescence detection.

  Electrophoresis 20050801

• Degradation of 3,4-dichloro- and 3,4-difluoroaniline by Pseudomonas fluorescens 26-K.

  Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 20030301