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3225-97-6

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3225-97-6 Usage

General Description

1-amino-4-chloro-2-methylanthraquinone is a chemical compound with the molecular formula C15H10ClNO2. It is an organic compound that contains an anthraquinone structure, which is commonly used in the production of dyes and pigments. This particular compound is a derivative of anthraquinone, with a chlorine atom at the 4-position and an amino group at the 1-position, as well as a methyl group at the 2-position. It is a dark reddish-brown solid that is insoluble in water but soluble in organic solvents. 1-amino-4-chloro-2-methylanthraquinone is known for its high lightfastness and is used in the production of high-quality industrial dyes and as a coloring agent in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3225-97-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3225-97:
(6*3)+(5*2)+(4*2)+(3*5)+(2*9)+(1*7)=76
76 % 10 = 6
So 3225-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClNO2/c1-7-6-10(16)11-12(13(7)17)15(19)9-5-3-2-4-8(9)14(11)18/h2-6H,17H2,1H3

3225-97-6SDS

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 1-amino-4-chloro-2-methylanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1-Amino-4-chlor-2-methyl-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:3225-97-6 SDS

3225-97-6Relevant articles and documents

TRANSFORMATIONS OF ANTHRAISOXAZOL-6-ONES IN HYDROHALIC ACIDS

Gornostaev, L. M.,Sakilidi, V. T.

, p. 1112 - 1114 (2007/10/02)

4-Halo-1-aminoanthraquinones are formed when anthraisoxazol-6-ones are refluxed in hydrohalic acids.The 3 position undergoes halogenation when 5-substituted isoxazoles are used.The process takes place via a one-proton mechanism with the participation of halide ion in the rate-determining step, possibly with the intermediate formation of N-haloaminoanthraquinones.

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