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6994-46-3

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6994-46-3 Usage

Preparation

(a) 1,4-Dihydroxyanthracene-9,10-dione and Ethanamine (2 Moore) condensation; (b) 1,4-Diamino anthraquinone and Chloroethane or Bromoethane condensation.

Properties and Applications

brilliant red light blue. Used for hydrocarbon solvent, grease, paraffin wax, petroleum products, polystyrene and paint color. Standard Light Fastness Heat-resistant(℃) water Sodium Carbonate(5%) Hydrochloric acid(5%) Melting point Stable ISO Good 260 Insoluble

Standard

Light Fastness

Melting point

Stable

ISO

Good

Check Digit Verification of cas no

The CAS Registry Mumber 6994-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6994-46:
(6*6)+(5*9)+(4*9)+(3*4)+(2*4)+(1*6)=143
143 % 10 = 3
So 6994-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H18N2O2/c1-3-19-13-9-10-14(20-4-2)16-15(13)17(21)11-7-5-6-8-12(11)18(16)22/h5-10,19-20H,3-4H2,1-2H3

6994-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(ethylamino)anthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names Atlasol Blue 2N

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:6994-46-3 SDS

6994-46-3Downstream Products

6994-46-3Relevant articles and documents

Phase transfer catalysed N-monoalkylation of amino anthraquinones

Ramrao,Ramkumar,Anant,Ramanuja

, p. 1129 - 1135 (2007/10/02)

1-Alkylaminoanthraquinones (2a-f) and 1,4-bisalkylaminoanthraquinones (4a-c) were prepared from aminoanthraquinones (1,3) by alkylation with alkyl sulphate/alkyl halide in presence of powdered sodium hydroxide, potassium carbonate and phase transfer catalyst.

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