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66181-84-8

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66181-84-8 Usage

Preparation

1,4,5,8-Tetrachloroanthracene-9,10-dione and aniline (4 Moore) condensation.

Check Digit Verification of cas no

The CAS Registry Mumber 66181-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,8 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66181-84:
(7*6)+(6*6)+(5*1)+(4*8)+(3*1)+(2*8)+(1*4)=138
138 % 10 = 8
So 66181-84-8 is a valid CAS Registry Number.
InChI:InChI=1/C38H28N4O2/c43-37-33-29(39-25-13-5-1-6-14-25)21-22-30(40-26-15-7-2-8-16-26)34(33)38(44)36-32(42-28-19-11-4-12-20-28)24-23-31(35(36)37)41-27-17-9-3-10-18-27/h1-24,39-42H

66181-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5,8-tetraanilinoanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,4,5,8-Tetrakis(phenylamino)anthraquinone

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:66181-84-8 SDS

66181-84-8Downstream Products

66181-84-8Relevant articles and documents

Method for catalytically synthesizing N-aryl/alkyl anthraquinone and derivatives thereof by using carbene metal ligand

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Paragraph 0015, (2020/07/13)

The invention discloses a method for catalytically synthesizing N-aryl/alkyl anthraquinone and derivatives thereof by using a carbene metal ligand. The method for catalytically synthesizing the N-aryl/alkyl anthraquinone and the derivatives thereof by using the carbene metal ligand provided by the invention comprises the following steps: with the carbene metal ligand and alkali as catalysts and anthraquinone compounds and primary amine compounds as raw materials, allowing the anthraquinone compounds and the primary amine compounds to react in an organic solvent at 100-150 DEG C for 2-12 hours;cooling a reaction liquid after the reaction is finished, and carrying out rotary evaporation so as to remove the solvent; purifying a crude product through a silicon dioxide column, and carrying outeluting with petroleum ether/dichloromethane so as to obtain pure N-aryl/alkyl anthraquinone and derivatives thereof. According to the invention, the selectivity of a tetra-substituted target productis improved and is 90% or above; byproducts are few, and the separation cost of a product is reduced; the reaction is carried out in the organic solvent without water and oxyge;, simple reaction conditions and easy operation are achieved; and industrial production is facilitated.

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