15539-29-4

Basic information

• Product Name: 9-propylacridine
• Synonyms: 9-propylacridine
• CAS NO: 15539-29-4
• Molecular Formula: C16H15N
• Molecular Weight: 221.297
• Mol File: 15539-29-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 9-propylacridine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-propylacridine(15539-29-4)
• EPA Substance Registry System: 9-propylacridine(15539-29-4)

Safety Data

• Hazardous Substances Data: 15539-29-4(Hazardous Substances Data)

Upstream product

• 122-39-4 diphenylamine 
• 107-92-6 butyric acid 
• 260-94-6 acridine 
• 65753-73-3 9-propyl-9,10-dihydroacridine 

Relevant articles and documents

Intermolecular ferromagnetic interaction in the crystal of a diphenyl nitroxide derivative. The role of spin-polarized hydrogen atoms located near a neighboring N-O site

The crystal of 9,9-dipropyl-9,10-dihydroacridin-10-yloxyl exhibited a positive Weiss constant (+0.77 K) ascribable to a three-dimensional network of ferromagnetic interactions. The orbital orthogonality between the antibonding N-O π* and H 1s orbitals was found in a nearly isosceles triangle geometry of neighboring H atoms and the N-O site. The following spin polarization scheme is proposed: N(↑)-C(↓)=Co(↑)-Cm(↓)-H m(↑)O(↑)-N, where o- and m-positions are defined with respect to the N-O group.

Deactivation Mechanism of Excited Acridine and 9-Substituted Acridines in Water

The deactivation processes of excited acridine, deuterated acridine, and 9-substituted acridines (9-methyl, 9-propyl, 9-chloro, and 9-amino) have been investigated in alkaline and acidic water.The photoreaction does not occur with the irradiation of 365-n

9-alkylacridine synthesis using 2,2-dimethoxypropane as water scavenger

A rapid and high yielding green method was developed for acridine derivative synthesis in solvent free medium. The commercial reagents are easily converted into products by using of microwaves in a heterogeneous medium in the presence of zinc chloride and 2,2-dimethoxypropane. Principal advantages of the procedure are short time, low energy consumption, and easy work-up.

Rapid synthesis of acridines using microwave

Microwave irradiation for several minutes caused reaction of diarylamines with carboxylic acids in the presence of zinc chloride to give 9-substituted acridines in good yield.