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2177-10-8

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2177-10-8 Usage

Type of compound

Derivative of anthraquinone

Common uses

Production of dyes and pigments

Functional groups

Nitro group, amino group, hydroxyl groups at positions 4 and 8

Structural features

Nitro and amino groups attached to anthraquinone backbone

Chemical properties

Ability to form complexes with metal ions

Color-changing properties

Exhibits color-changing properties due to functional groups

Applications

Chemical and pharmaceutical industries

Synthesis

Used as an intermediate in the synthesis of other organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 2177-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2177-10:
(6*2)+(5*1)+(4*7)+(3*7)+(2*1)+(1*0)=68
68 % 10 = 8
So 2177-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H8N2O6/c15-5-1-3-7(17)11-9(5)13(19)12-8(18)4-2-6(16(21)22)10(12)14(11)20/h1-4,17-18H,15H2

2177-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-4,8-dihydroxy-5-nitroanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 4-Amino-8-nitroanthrarufin

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:2177-10-8 SDS

2177-10-8Downstream Products

2177-10-8Relevant articles and documents

Production of aminonitrodihydroxyanthraquinones by partial reduction dinitrodihydroxyanthraquinones

-

, (2008/06/13)

The production of aminonitrodihydroxyanthraquinones of the formula: STR1 in which one X is OH and the other X is NO2 by partial reduction of the corresponding dinitrodihydroxyanthraquinone or mixtures thereof by heating at 80°-250° C in the presence of 1/2 to 5 times the weight thereof of an unsubstituted or substituted phenol. The reduction is accelerated by being carried out in the presence of a small amount such as 0.5-20 mol percent of an alkaline-reacting agent. Pure aminonitrohydroxyanthraquinones are obtained which are free from diaminodihydroxyanthraquinones.

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