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84-46-8

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84-46-8 Usage

General Description

2-amino-3-chloro-anthraquinon is a chemical compound that belongs to the anthraquinone group, which is commonly used in the production of dyes and pigments. It is a derivative of anthraquinone, with an amino group and a chlorine atom attached to the third and second carbon atoms, respectively. 2-amino-3-chloro-anthraquinon is known for its intense red color and is often used in the textile industry to dye fabrics and fibers. Additionally, 2-amino-3-chloro-anthraquinon has also been investigated for its potential anti-tumor and anti-inflammatory properties, making it of interest for pharmaceutical and medical research.

Check Digit Verification of cas no

The CAS Registry Mumber 84-46-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84-46:
(4*8)+(3*4)+(2*4)+(1*6)=58
58 % 10 = 8
So 84-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H8ClNO2/c15-11-5-9-10(6-12(11)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,16H2

84-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,10-Anthracenedione,2-amino-3-chloro-

1.2 Other means of identification

Product number -
Other names 2-Amino-3-chlor-anthrachinon

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:84-46-8 SDS

84-46-8Relevant articles and documents

PHOTOCHEMICAL REACTION OF 9,10-ANTHRAQUINONE AND ITS DERIVATIVES WITH PYRIDINE

Loskutov, V.A.,Lukonina, S.M.,Konstantinova, A.V.,Fokin, E.P.

, p. 500 - 504 (2007/10/02)

The previously unknown photochemical reaction of 9,10-anthraquinone with pyridine in an atmosphere of argon takes place with formation of 2-(1,2-dihydropyridino)- or 2-(1,4-dihydropyridino)-9,10-anthraquinone, which is converted by the action of alkali into 2-aminoanthraquinone.In the presence of atmospheric oxygen the reaction product after treatment whith alkali is 1-aminoanthraquinone in addition to 2-aminoanthraquinone.The 1- and 2-methoxyanthraquinones and chloroanthraquinones react with pyridine in the light and form, after treatment with alkali, substituted aminoanthraquinones.

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