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2-Naphthalenol, 1-[(2-methyl-5-nitrophenyl)azo]- is an organic compound characterized by its azo group, which is a diazenyl functional group (-N=N-). This particular compound features a naphthalenol core, which is a derivative of naphthalene, a two-ring aromatic hydrocarbon. The molecule is further defined by the presence of a methyl group at the 2-position and a nitro group at the 5-position of the phenyl ring attached to the azo group. This chemical structure gives the compound unique properties and potential applications in various fields, such as dyes and pigments, due to its ability to absorb and reflect light. It is important to note that the compound's specific properties, such as solubility, stability, and reactivity, can be influenced by the presence of these functional groups and the overall molecular structure.

6410-15-7

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6410-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6410-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6410-15:
(6*6)+(5*4)+(4*1)+(3*0)+(2*1)+(1*5)=67
67 % 10 = 7
So 6410-15-7 is a valid CAS Registry Number.

6410-15-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-Methyl-5-nitrophenyl)diazenyl]-2-naphthol

1.2 Other means of identification

Product number -
Other names 2-Pyridinemethanol,4-nitro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6410-15-7 SDS

6410-15-7Downstream Products

6410-15-7Relevant academic research and scientific papers

A quantitative one-pot synthesis method for industrial azo pigments with recyclable wastewater

Feng, Guangyuan,Zhu, Meiling,Liu, Lei,Li, Chunbao

supporting information, p. 1769 - 1776 (2019/04/08)

Most industrial azo pigments are synthesized by diazotization in one pot and then coupling in another. This two-pot process has been transformed into a one-pot method by adding granular PTFE (polytetrafluoroethylene) to a mechanically agitated aqueous mixture of NaNO2, HCl, a diazo component and a coupling component. This method avoids the step of using a base or a surfactant to dissolve the coupling component. The reactions were fast and quantitative. The granular PTFE, wastewater and excess HCl were then reused 11 times without deteriorating the reaction rate and product purity. Altogether, 22 industrial pigments and 3 azo compounds were synthesized and the reaction can produce up to 22.7 g of product in the laboratory. Some reactions require less than 2 equiv. of HCl and a mechanism explaining this is proposed. In addition, an o-nitro group effect is advanced to explain the differences in coupling reaction rates for o-, m- and p-nitroaniline.

Method used for synthesizing azo compound using solid particle one kettle method

-

Paragraph 0127; 0128; 0129, (2019/01/07)

The invention relates to a method used for synthesizing an azo compound using solid particle one kettle method. The method comprises following steps: solid particles are introduced into a reaction container, an inorganic acid, an aromatic primary amine, sodium nitrite, water, and a coupling component are added, mechanism stirring is carried out, when the reaction is monitored to be finished, filtering and rinsing are carried out, and the obtained filter cake is a finished product; or the solid particles are introduced into the reaction container, the inorganic acid, the aromatic primary amine,sodium nitrite, and water are added, mechanical stirring is carried out, after complete conversion of the aromatic primary amine, the coupling component is added, mechanical stirring is carried out,when the reaction is monitored to be finished, filtering and rinsing are carried out, and the obtained filter cake is a finished product. The solid particles are preferably selected from polytetrafluoroethylene particles, haw seeds, or stainless steel sand. The solid particles are added into the reaction system to promote reaction, no pre-heating or alkali adding dissolving of diazo components orthe coupling component is needed; most reaction is finished in 1h; reaction time is short; product quality is high; and reaction filtrate and excess inorganic acid can be recycled for a plurality of times.

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