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Naphth[2,3-c]acridine-5,8,14(13H)-trione is a complex organic compound with the molecular formula C21H11NO3. It is a tricyclic aromatic compound, featuring a naphthalene ring fused to an acridine ring, with three carbonyl groups (C=O) at the 5, 8, and 14 positions. Naphth[2,3-c]acridine-5,8,14(13H)-trione is known for its potential applications in the field of medicinal chemistry, particularly as a scaffold for the development of new drugs. Its chemical structure allows for a range of functional group modifications, which can lead to the synthesis of various derivatives with different biological activities. The compound's name reflects its unique structure, with "naphtho" indicating the presence of a naphthalene ring, "acridine" referring to the acridine core, and the numbers and suffixes specifying the positions of the carbonyl groups and the hydrogen atoms.

3569-01-5

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3569-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3569-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3569-01:
(6*3)+(5*5)+(4*6)+(3*9)+(2*0)+(1*1)=95
95 % 10 = 5
So 3569-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H11NO3/c23-19-11-5-1-2-6-12(11)21(25)17-14(19)9-10-15-18(17)22-16-8-4-3-7-13(16)20(15)24/h1-10H,(H,22,24)

3569-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 13H-naphtho[2,3-c]acridine-5,8,14-trione

1.2 Other means of identification

Product number -
Other names Naphtho[2,3-c]acridine-5,8,14(13H)-trione

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 -
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More Details:3569-01-5 SDS

3569-01-5Relevant academic research and scientific papers

Synthesis and Transformations of 3-Aroylanthraisoxazol-6-ones

Gornostaev, L. M.,Levdanskii, V. A.,Arnol'd, E. V.

, p. 19 - 21 (2007/10/02)

3-Aroylanthraisoxazol-6-ones (II) are formed when 1-azido-2-aroylanthraquinones are refluxed in o-dichlorobenzene; this may constitute evidence that reactions of this type proceed via a "concerted" mechanism.Thermolysis of these and other substances in nitrobenzene leads to 7,8-phthaloylacridones, the structures of which were confirmed by alternative synthesis.

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