5959-56-8 Usage
Description
4-Amino-1-naphthol hydrochloride is an organic compound with the chemical formula C10H9NO·HCl. It is a pink to grey powder and is known for its use in the synthesis of various chemical compounds.
Uses
Used in Chemical Synthesis:
4-Amino-1-naphthol hydrochloride is used as a chemical intermediate for the synthesis of various compounds. It serves as a building block in the creation of different organic molecules, contributing to the development of new materials and products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Amino-1-naphthol hydrochloride is used as a key component in the synthesis of 2-(3-aminophenol)-6-(4-amino-1-naphthol)-4-chloro-s-triazine. 4-Amino-1-naphthol hydrochloride has potential applications in the development of pharmaceuticals, particularly those with therapeutic properties.
Used in Dye and Pigment Industry:
4-Amino-1-naphthol hydrochloride is also utilized in the synthesis of 4-aminoalkyl-1-naphthol derivatives, which are important for the production of dyes and pigments. These derivatives are valuable in the creation of vibrant and stable colors for various applications, including textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 5959-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5959-56:
(6*5)+(5*9)+(4*5)+(3*9)+(2*5)+(1*6)=138
138 % 10 = 8
So 5959-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO.ClH/c11-9-5-6-10(12)8-4-2-1-3-7(8)9;/h1-6,12H,11H2;1H
5959-56-8Relevant articles and documents
A simple reduction method of azo-compounds to amines using Fe powder in the presence of NH4Cl
Mobinikhaledi, Akbar,Foroughifar, Naser,Jirandehi, Hasan Fathinejad
, p. 755 - 757 (2008/02/09)
A series of azo-compounds were reduced to related aromatic amines in the presence of Fe powder and ammonium chloride. This one step protocol led to the formation of products in middle to high yields, especially when electron releasing substituted aromatic azo-compounds were reduced.
