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"10-[3-(dimethylamino)propyl]-2-methoxyacridin-9(10H)-one" is a complex organic compound with a molecular formula of C20H24N2O2. It is a derivative of acridine, a tricyclic compound with a central nitrogen atom. The structure features a dimethylaminopropyl group attached to the 10th position, and a methoxy group at the 2nd position. 10-[3-(dimethylamino)propyl]-2-methoxyacridin-9(10H)-one is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of certain drugs. Its chemical properties and reactivity are influenced by the presence of the amine and methoxy groups, which can participate in various chemical reactions, such as nucleophilic substitutions and acid-base reactions. The compound's specific role and effectiveness in pharmaceuticals are areas of ongoing research and development.

77213-55-9

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77213-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77213-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,1 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77213-55:
(7*7)+(6*7)+(5*2)+(4*1)+(3*3)+(2*5)+(1*5)=129
129 % 10 = 9
So 77213-55-9 is a valid CAS Registry Number.

77213-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-[3-(dimethylamino)propyl]-2-methoxyacridin-9-one

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:77213-55-9 SDS

77213-55-9Downstream Products

77213-55-9Relevant academic research and scientific papers

Alkylation et acetylation d'acridanones. Cas de la methoxy-2 acridanone-9

Chaffia, Brat Ali,Montginoul, Claude,Toreilles, Eliane,Giral, Louis

, p. 345 - 350 (2007/10/02)

The interest of the N-alkylacridanone derivatives lies in their biological properties.We describe the results of various substitution reactions of 2-methoxy-9-acridanone.This substrate, previously metallated by sodium hydride, was reacted with alkyl, allyl, crotyl and benzyl halides and also with alkylamino and acetyl halides in dimethylformamide.A mixture of O-alkyl and N-alkyl isomers, or only one of them, was obtained.The reaction products are interpreted in terms of hardness and softness of reacting centres.

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