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606-41-7

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606-41-7 Usage

General Description

2-amino-1-naphthol is an organic chemical compound with the molecular formula C10H9NO. It is a derivative of naphthol and contains an amino group, giving it both aromatic and basic properties. 2-amino-1-naphthol is commonly used in the production of dyes, specifically azo dyes, as it easily undergoes diazotization and coupling reactions to form a wide range of colorants. Additionally, 2-amino-1-naphthol has applications in the manufacturing of pharmaceuticals and as a reagent in organic synthesis. It is important to handle this chemical with care, as it can be toxic and poses potential health hazards if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 606-41-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 606-41:
(5*6)+(4*0)+(3*6)+(2*4)+(1*1)=57
57 % 10 = 7
So 606-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6,12H,11H2

606-41-7SDS

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 2-aminonaphthalen-1-ol

1.2 Other means of identification

Product number -
Other names 2-aminonaphthol

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:606-41-7 SDS

606-41-7Relevant articles and documents

Degradation of azo dye, acid red-14 by hexacyanoferrate(III) using iridium nanoclusters: A kinetic study

Lasyal, Rajni,Goel, Anjali

, p. 335 - 338 (2016)

In the present work, a novel method for the treatment of wastewater containing an azo dye, acid red-14 by hexacyanoferrate [HCF(III)] in presence of iridium nanoclusters has been proposed. The effect of some important operational parameters such as pH, temperature and catalyst concentration (iridium nano) has been investigated by kinetic spectrophotometric method at λmax 515 nm of the reaction mixture. The results reveal that degradation kinetics of acid red-14 follows first order kinetic model with respect to [HCF(III)], [acid red-14] and Ir nano concentration. Iridium nanoclusters were recovered with the help of centrifugation and reused for three consecutive cycles. Thermodynamic parameters Ea, ΔS#, ΔF#, ΔH# and 'A' have been calculated by studying the reaction rate in the range of temperatures 40 to 55 °C. The formation of degradation products was characterized by chromatographic and spectroscopic techniques after the extraction with ethyl acetate. 1-Hydroxy-2-amino naphthalene and naphthalene sodium sulphate were identified as major degradation products. The results can provide fundamental knowledge for the treatment of wastewater containing acid red-14/other azo dyes.

Regio- and chemoselective catalytic transfer hydrogenation of aromatic nitro and carbonyl as well as reductive cleavage of azo compounds over novel mesoporous NiMCM-41 molecular sieves

Mohapatra, Susanta K.,Sonavane, Sachin U.,Jayaram, Radha V.,Selvam, Parasuraman

, p. 4297 - 4300 (2007/10/03)

(equation presented) Regio-and chemoselective reduction of nitroarenes and carbonyl compounds and reductive cleavage of azo compounds, including bulkier molecules, was achieved by the catalytic transfer hydrogenation method (CTH) using a novel nickel-containing mesoporous silicate (NiMCM-41) molecular sieve catalyst. In addition, the catalyst was also found to behave as a truly heterogeneous catalyst as the yield was practically unaffected.

Method for preparing adduct of butadiene polymer or copolymer and α, β-ethylenically unsaturated dicarboxylic acid compound

-

, (2008/06/13)

In a method for preparing an adduct of (A) a butadiene lower polymer or butadiene lower copolymer and (B) a α,β-ethylenically unsaturated dicarboxylic acid compound, said method is characterized in that said (A) and (B) are caused to react in the presence of one or more compounds selected from (C) p-phenylenediamine derivatives, catechol derivatives, pyrogallol derivatives, N-nitrosamines, quinoline derivatives and naphthol derivatives, thus serious increase of the viscosity of said adduct in the addition reaction can be prevented.

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