71535-97-2

Basic information

• Product Name: 2,2',4,4'-TETRANITROBENZOPHENONE
• Synonyms: 2,2',4,4'-TETRANITROBENZOPHENONE;Bis(2,4-dinitrophenyl)Methanone;NSC 28668;NSC 48920
• CAS NO: 71535-97-2
• Molecular Formula: C₁₃H₆N₄O₉
• Molecular Weight: 362.21
• Product Categories: Fluorescent Labels & Indicators
• Mol File: 71535-97-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 230°C
• Boiling Point: 650.2°Cat760mmHg
• Flash Point: 334.3°C
• Appearance: /
• Density: 1.685g/cm³
• Vapor Pressure: 8.64E-17mmHg at 25°C
• Refractive Index: 1.69
• Storage Temp.: -20°C Freezer
• Solubility: Acetonitrile (Slightly, Heated), DMSO (Slightly)
• CAS DataBase Reference: 2,2',4,4'-TETRANITROBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2',4,4'-TETRANITROBENZOPHENONE(71535-97-2)
• EPA Substance Registry System: 2,2',4,4'-TETRANITROBENZOPHENONE(71535-97-2)

Safety Data

• Hazardous Substances Data: 71535-97-2(Hazardous Substances Data)

Usage

Chemical Properties

Pale Yellow Solid

Uses

2,2’,4,4’-Tetranitrobenzophenone (cas# 71535-97-2) is a compound useful in organic synthesis.

InChI:InChI=1/C13H6N4O9/c18-13(9-3-1-7(14(19)20)5-11(9)16(23)24)10-4-2-8(15(21)22)6-12(10)17(25)26/h1-6H

Upstream product

• 1817-76-1 2,2',4,4'-tetranitrodiphenylmethane 
• 64-19-7 acetic acid 
• 101-81-5 Diphenylmethane 

Downstream Products

• 71503-90-7 3,6-dinitro-10-p-tolylacridin-9-one 
• 154010-53-4 2',4,4'-trinitro-2'-p-toluidinobenzophenone 
• 154010-63-6 2-p-chloroanilino-2',4,4'-trinitrobenzophenone 
• 154010-55-6 2-chloro-6-nitro-9-(2,4-dinitrophenyl)acridine 
• 154010-56-7 2-methyl-6-nitro-9-(2,4-dinitrophenyl)acridine 
• 154010-65-8 3-nitro-9-(2,4-dinitrophenyl)acridine 
• 71642-43-8 3,6-diphenoxy-10-phenylacridin-9-one 
• 166405-61-4 9-phenyl-3,6-bis<(ethoxycarbonyl)amino>acridine 
• 58067-04-2 9-phenyl-acridine-3,6-diamine 
• 351351-75-2 N-[9-(4-dimethylamino-phenylamino)-6-(3-pyrrolidin-1-yl-propionylamino)-acridin-3-yl]-3-pyrrolidin-1-yl-propionamide 

Relevant articles and documents

Fluorinated 3,6,9-trisubstituted acridine derivatives as DNA interacting agents and topoisomerase inhibitors with A549 antiproliferative activity

A series of new 3,6,9-trisubstituted acridine derivatives with fluorine substituents on phenyl ring were synthesized and their interaction with calf thymus DNA was investigated. Analysis using UV–Vis absorbance spectra provided valuable information about

Structure-based design of benzylamino-acridine compounds as G-quadruplex DNA telomere targeting agents

The design, synthesis, biophysical and biochemical evaluation is presented of a new series of benzylamino-substituted acridines as G-quadruplex binding telomerase inhibitors. Replacement of the previously reported anilino substituents by benzylamino group

Therapeutic acridone and acridine compounds

The present invention pertains to acridone and acridine compounds of formula (I), wherein either: (a) K is ═O, L is —H, alpha is a single bond, beta is a double bond, gamma is a single bond (acridones); or, (b) K is a 9-substituent, L is absent, alpha is