1198-27-2 | 1-Amino-2-naphthol, HCl

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$53.00	$38.00
5g	95%	in stock	$147.00	$103.00
25g	95%	in stock	$504.00	$353.00

Description

• Catalog Number: AA33066
• Chemical Name: 1-Amino-2-naphthol, HCl
• CAS Number: 1198-27-2
• Molecular Formula: C10H10ClNO
• Molecular Weight: 195.6455
• MDL Number: MFCD00012561
• SMILES: Oc1ccc2c(c1N)cccc2.Cl

Computed Properties

• Complexity: 160
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 3

Upstream Synthesis Route

1-Aminonaphthalen-2-ol hydrochloride is a versatile chemical compound commonly used in chemical synthesis processes. This compound is valued for its ability to serve as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.Its unique structure and properties make it a valuable reagent in the synthesis of complex organic molecules. 1-Aminonaphthalen-2-ol hydrochloride can be utilized as a precursor in the production of heterocyclic compounds, which are essential in drug discovery and development. Its presence in synthesis reactions can facilitate the formation of carbon-carbon and carbon-nitrogen bonds, enabling the construction of intricate chemical structures.Furthermore, 1-Aminonaphthalen-2-ol hydrochloride plays a crucial role in the preparation of dyes, pigments, and fine chemicals. Its reactivity and functional groups allow for various derivatization strategies, leading to the creation of diverse chemical products with desired properties.Overall, the application of 1-Aminonaphthalen-2-ol hydrochloride in chemical synthesis underscores its importance in the field of organic chemistry and highlights its potential for contributing to the development of innovative molecules with wide-ranging industrial applications.

Literature

• Evaluation of impact of exposure of Sudan azo dyes and their metabolites on human intestinal bacteria.

  Anaerobe 20120801

• Effects of Orange II and Sudan III azo dyes and their metabolites on Staphylococcus aureus.

  Journal of industrial microbiology & biotechnology 20111001

• Decolorization of azo dyes in bioelectrochemical systems.

  Environmental science & technology 20090701

• Structural and temperature effects in the high-performance liquid chromatographic enantioseparation of 1-(alpha-aminobenzyl)-2-naphthol and 2-(alpha-aminobenzyl)-1-naphthol analogs.

  Journal of separation science 20051201