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52821-24-6

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52821-24-6 Usage

Description

2-(3-hydroxypropyl)-6-[(3-hydroxypropyl)amino]-1H-benz[de]isoquinoline-1,3(2H)-dione is a yellow powder with a greenish shade. It has a density of 1.20 g/cm3 and a tinging strength of 100-105%. 2-(3-hydroxypropyl)-6-[(3-hydroxypropyl)amino]-1H-benz[de]isoquinoline-1,3(2H)-dione has a heat resistance of 200°C and shows light fastness and water resistance of 5. It also has a low water solubility of 1.0% max and a residue on 80 mesh of 5.0% max. 2-(3-hydroxypropyl)-6-[(3-hydroxypropyl)amino]-1H-benz[de]isoquinoline-1,3(2H)-dione has a volatile content of 1.0% max at 105°C and a weight metal total of 50ppm max.

Uses

Used in Pharmaceutical Industry:
2-(3-hydroxypropyl)-6-[(3-hydroxypropyl)amino]-1H-benz[de]isoquinoline-1,3(2H)-dione is used as a pharmaceutical compound for its potential therapeutic applications. Its chemical structure and properties make it a promising candidate for the development of new drugs.
Used in Chemical Industry:
2-(3-hydroxypropyl)-6-[(3-hydroxypropyl)amino]-1H-benz[de]isoquinoline-1,3(2H)-dione is used as a chemical intermediate for the synthesis of various compounds. Its unique structure and functional groups can be utilized in the production of different chemicals and materials.
Used in Research and Development:
2-(3-hydroxypropyl)-6-[(3-hydroxypropyl)amino]-1H-benz[de]isoquinoline-1,3(2H)-dione is used as a research compound for studying its chemical properties, reactivity, and potential applications in various fields. Its unique structure and properties make it an interesting subject for scientific investigation.

Flammability and Explosibility

Notclassified

TEST ITEMS

SPECIFICATION

HEAT RESISTANCE

200 °C min

LIGHT FASTNESS

5

ACID RESISTANCE

4

ALKALI RESISTANCE

4

RESIDUE ON 80 MESH

5.0% max

VOLATITE 105 °C

1.0% max

WEIGHT METAL TOTAL

50ppm max

Check Digit Verification of cas no

The CAS Registry Mumber 52821-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,2 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52821-24:
(7*5)+(6*2)+(5*8)+(4*2)+(3*1)+(2*2)+(1*4)=106
106 % 10 = 6
So 52821-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O4/c21-10-2-8-19-15-7-6-14-16-12(15)4-1-5-13(16)17(23)20(18(14)24)9-3-11-22/h1,4-7,19,21-22H,2-3,8-11H2

52821-24-6SDS

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 2-(3-hydroxypropyl)-6-(3-hydroxypropylamino)benzo[de]isoquinoline-1,3-dione

1.2 Other means of identification

Product number -
Other names 4-(3-Hydroxypropylamino)-naphthal(3-hydroxypropyl)imide

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:52821-24-6 SDS

52821-24-6Downstream Products

52821-24-6Relevant articles and documents

Synthesis of hydroxyl containing N-imides of 4-substituted naphthalic acid

Minakova,Bedrik,Shershukov,Surov,Pivnenko

, p. 621 - 624 (1999)

A convenient, one-step method for synthesis of the N-(3-hydroxypropyl)imide of 4-(3′-hydroxypropyl)-aminonaphtalic acid is proposed. It has been found that ethylene glycol monoethyl ether can be successfully used to replace solvents previously used for these reactions. 1999 KluwerAcademic/Plenum Publishers.

The synthesis and fluorescence of novel N-substituted-1,8-naphthylimides

Yuan, Dongwu,Brown, Robert G.,Hepworth, John D.,Alexiou, Michael S.,Tyman, John H. P.

, p. 397 - 404 (2008/09/20)

(Chemical Equation Presented) The synthesis and characterisation of a series of novel 4-acylamino and 4-alkylamino-N-1,8-naphthalimides is described. The UV-visible absorption and emission properties of the compounds are reported. Significant solvent effects are noted for 4-n-butyl-9-n-butyl-1,8- naphthylimide. The incorporation of acetyl and chloroacetyl groups into the 4-substituent markedly increases the fluorescence quantum yield compared with 4-alkylamino substituemnts.

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