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1758-64-1

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1758-64-1 Usage

Type of compound

Derivative of anthraquinone

Applications

a. Synthesis of dyes and pigments
b. Production of reactive dyes for textiles
c. Production of colorants for inks, paints, and coatings
d. Pharmaceutical production
e. Reagent in organic synthesis in research laboratories

Color

Deep red-violet

Importance

a. Significant chemical in dye chemistry
b. Crucial in materials science

Versatility

Used in various industries due to its vibrant color and multiple applications

Check Digit Verification of cas no

The CAS Registry Mumber 1758-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1758-64:
(6*1)+(5*7)+(4*5)+(3*8)+(2*6)+(1*4)=101
101 % 10 = 1
So 1758-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O2/c15-7-4-5-8-10(6-7)13(17)9-2-1-3-11(16)12(9)14(8)18/h1-6H,15-16H2

1758-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-diaminoanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 9,1,6-diamino

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:1758-64-1 SDS

1758-64-1Relevant articles and documents

Process for the preparation of fluoroaromatic and fluoroheteroaromatic compounds

-

, (2008/06/13)

Good yields of a range of fluoroaromatic and fluoroheteroaromatic compounds may be obtained by reacting an aromatic or a heteroaromatic amine with a nitrosyl polyfluoro salt in an inert solvent to form an intermediate aryl or heteroaryl diazonium polyfluoro salt and decomposing this aryl or heteroaryl diazonium polyfluoro salt in situ. The process described is especially suitable for the preparation in good yield of fluoroaromatic and fluoroheteroaromatic compounds with ortho substituents.

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