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3300-23-0

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3300-23-0 Usage

Structure

A derivative of anthracene, a polycyclic aromatic hydrocarbon

Appearance

Dark yellow solid

Usage

Commonly used in the synthesis of various organic compounds

Potential applications

a. Organic electronic materials
b. Precursor for the synthesis of dyes and pigments
c. Medicinal chemistry (further research needed)

Properties

Versatile building block for organic synthesis

Fields of application

Various fields of science and technology

Check Digit Verification of cas no

The CAS Registry Mumber 3300-23-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3300-23:
(6*3)+(5*3)+(4*0)+(3*0)+(2*2)+(1*3)=40
40 % 10 = 0
So 3300-23-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H8BrNO2/c15-10-6-5-9-11(12(10)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,16H2

3300-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-2-bromoanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1-Amino-2-brom-anthrachinon

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:3300-23-0 SDS

3300-23-0Relevant articles and documents

SUBSTITUTION OF A HYDROGEN ATOM IN 6-OXO-6H-ANTHRAISOXAZOLES BY ALKYL PHENYL ETHERS AND ALKYLBENZENES

Gornostaev, L. M.,Es'kin, A. P.,El'tsov, A. V.

, p. 2352 - 2357 (2007/10/02)

During the reaction of 3-bromo-6-oxo-6H-anthraisoxazole with alkyl phenyl ethers in the presence of aluminum chloride a hydrogen atom is substituted with the formation of the corresponding 4-aryl-substituted 1-aminoanthraquinones; the reactions wi

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