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65869-69-4

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65869-69-4 Usage

Class of organic compounds

Anthraquinones

Physical state

Dark brown solid

Common uses

a. Dye intermediate for textiles and paper
b. Synthesis of pharmaceuticals and agrochemicals

Potential applications

a. Organic semiconductor in electronic devices
b. Organic light-emitting diodes (OLEDs)
c. Organic field-effect transistors (OFETs)

Safety precautions

a. Harmful if ingested or inhaled
b. Can cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 65869-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,6 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65869-69:
(7*6)+(6*5)+(5*8)+(4*6)+(3*9)+(2*6)+(1*9)=184
184 % 10 = 4
So 65869-69-4 is a valid CAS Registry Number.

65869-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dihydroxypentacene-5,14-dione

1.2 Other means of identification

Product number -
Other names 1,4-Dihydroxy-5,14-pentacenchinon

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:65869-69-4 SDS

65869-69-4Downstream Products

65869-69-4Relevant articles and documents

Capture du paradimethoxyorthoquinodimethane:syntheses de quinones et d'un intermediaire de la daunomycinone

Laduranty, Joelle,Lepage, Lucette,Lepage, Yves

, p. 1161 - 1167 (2007/10/02)

New para-dimethoxyl and para-diacetoxy derivatives in the naphthalene, anthracene, naphthacene, naphtho(2,3-c)thiophene and benzo-c-thiophene series are synthesized via the trapping of o-quinodimethanes by various dienophiles.Among these compounds, and in

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