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N-Heptyl-9-acridinamine is an organic compound with the chemical formula C17H24N2. It is a derivative of acridine, a tricyclic aromatic compound, and is characterized by the presence of a heptyl (seven-carbon) alkyl chain attached to the nitrogen atom at the 9th position of the acridine ring. N-Heptyl-9-acridinamine is known for its potential applications in the field of fluorescence, as it can exhibit strong fluorescence properties. It is also used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure and specific functional groups, N-heptyl-9-acridinamine is a subject of interest in chemical research and development, particularly in the areas of luminescent materials and medicinal chemistry.

7132-68-5

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7132-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7132-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7132-68:
(6*7)+(5*1)+(4*3)+(3*2)+(2*6)+(1*8)=85
85 % 10 = 5
So 7132-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H24N2/c1-2-3-4-5-10-15-21-20-16-11-6-8-13-18(16)22-19-14-9-7-12-17(19)20/h6-9,11-14H,2-5,10,15H2,1H3,(H,21,22)

7132-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-heptylacridin-9-amine

1.2 Other means of identification

Product number -
Other names acridin-9-yl-heptyl-amine

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:7132-68-5 SDS

7132-68-5Downstream Products

7132-68-5Relevant academic research and scientific papers

Synthesis and evaluation of N-alkyl-9-aminoacridines with antibacterial activity

Benoit, Adam R.,Schiaffo, Charles,Salomon, Christine E.,Goodell, John R.,Hiasa, Hiroshi,Ferguson, David M.

, p. 3014 - 3017 (2014/06/24)

A series of 9-alkylaminoacridines were synthesized and evaluated for activity against two strains of methicillin-resistant and one strain of methicillin-sensitive Staphylococcus aureus. Results are presented that show a clear structure activity relationship between the N-alkyl chain length and antibacterial activity with peak MIC99 values of 2-3 μM for alkyl chains ranging from 10 to 14 carbons in length. Although prior work has linked the function of acridine-based compounds to intercalation and topoisomerase inhibition, the present results show that 9-alkylaminoacridines likely function as amphiphilic membrane-active disruptors potentially in a similar manner as quaternary ammonium antimicrobials.

DIRECT SYNTHESIS OF SOME 9-AMINOALKYL ACRIDINES FROM 9-AMINO ACRIDINE USING PHASE TRANSFER CATALYSIS

Galy, Jean Pierre,Elguero, Jose,Vincent, Emile Jean

, p. 311 - 313 (2007/10/02)

A new method of preparation of 9-aminoalkyl acridines is described which avoid the use of 9-chloroacridine.Proton n.m.r. in trifluoroacetic acid easily differentiates 9-aminoalkyl from 9-amino 10-alkyl acridinium salts.Two dialkyl iminoacridanes have been

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