28767-75-1

Basic information

• Product Name: N1-(2,4-DINITRO-PHENYL)-ETHANE-1,2-DIAMINE
• Synonyms: N1-(2,4-DINITRO-PHENYL)-ETHANE-1,2-DIAMINE;N-(2,4-dinitrophenyl)ethylenediamine;4-(4-Morpholinyl-3-trifluoromethylaniline;2-diaMine;4-Dinitro-phenyl)-ethane-1;EDDnp;N-(2,4-Dinitro-phenyl)-ethane-1,2-diaMine;1,2-EthanediaMine, N1-(2,4-dinitrophenyl)-
• CAS NO: 28767-75-1
• Molecular Formula: C₈H₁₀N₄O₄
• Molecular Weight: 226.19
• Mol File: 28767-75-1.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 429.6 °C at 760 mmHg
• Flash Point: 213.6 °C
• Appearance: /
• Density: 1.48 g/cm³
• Vapor Pressure: 1.38E-07mmHg at 25°C
• Refractive Index: 1.67
• CAS DataBase Reference: N1-(2,4-DINITRO-PHENYL)-ETHANE-1,2-DIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N1-(2,4-DINITRO-PHENYL)-ETHANE-1,2-DIAMINE(28767-75-1)
• EPA Substance Registry System: N1-(2,4-DINITRO-PHENYL)-ETHANE-1,2-DIAMINE(28767-75-1)

Safety Data

• Hazardous Substances Data: 28767-75-1(Hazardous Substances Data)

Usage

Uses

N1-(2,4-Dinitrophenyl)ethane-1,2-diamine is a useful chemical reagent.

InChI:InChI=1/C8H10N4O4/c9-3-4-10-7-2-1-6(11(13)14)5-8(7)12(15)16/h1-2,5,10H,3-4,9H2

Upstream product

• 107-15-3 ethylenediamine 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 62024-69-5 N₁-(2,4-dinitrophenyl)ethane-1,2-diamine hydrochloride 
• 75008-95-6 5-amino-1-(2,4-dinitrophenyl)-1H-pyrazole-4-carbonitrile 
• 154853-46-0 2,4-dinitrophenyl 4-methoxybenzenesulfonate 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 89044-79-1 7-phenyl hexahydro-1,4-diazepine-5-one 
• 911209-11-5 C₁₃H₁₈N₄O₆ 

Downstream Products

• 23920-21-0 N-(2-(2,4-dinitrophenylamino)ethyl)acetamide 
• 169049-78-9 3',5'-di-O-acetyl-2'-deoxy-N₂-{2-[(2,4-dinitrophenyl)amino]ethyl}-O₆-[2-(4-nitrophenyl)ethyl]guanosine 
• 1332654-80-4 C₃₆H₅₄N₄O₆ 
• 1309804-33-8 C₁₁H₁₅N₄O₇P 
• 1309804-30-5 C₁₀H₁₆N₄O₁₀P₂ 
• 1309804-36-1 C₁₄H₂₃N₅O₁₀P₂ 
• 1224728-22-6 4-(3-amino-4-formylphenoxy)-N-(2-(2,4-dinitrophenylamino)ethyl)butanamide 
• 951312-87-1 tert-butyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-5-(2-(2,4-dinitrophenylamino)ethylamino)-5-oxopentanoate 

Relevant articles and documents

HAPTENS, HAPTEN CONJUGATES, COMPOSITIONS THEREOF AND METHOD FOR THEIR PREPARATION AND USE

A method for performing a multiplexed diagnostic assay, such as for two or more different targets in a sample, is described. One embodiment comprised contacting the sample with two or more specific binding moieties that bind specifically to two or more di

An all-organic steroid-D-π-A modular design drives ferroelectricity in supramolecular solids and nano-architectures at RT

Confluence of a modular design approach and self-assembly with a 'steroid-D-π-A' module generates spontaneous polarization in solids and for the first time in nano-architectures constituted from organogels, at room temperature (RT).

Facile solid-phase synthesis of AICAR 5-monophosphate (ZMP) and its 4-N-Alkyl derivatives

We report herein a facile, solid-phase synthesis of 5-aminol-β-D- ribofuranosylimidazole-4-carboxamide-5'-monophosphate (ZMP), a biosynthetic precursor of purine nucleotides, as well as a small collection of its 4-N-alkyl derivatives. The very difficult, direct, chemical phosphorylation of 5-amino-lβ-D-ribofuranosylimidazole-4-carboxamide (AICAR) was circumvented by installing a suitable, fully protected, phos phate group on the 5'-position of A-l-(2,4-dinitrophenyl)inosine, connected to the solid support through the 2',3'-positions, prior to the purine degradation, which led to the 5amino-imidazole-4-ca:rboxamide moiety. A plausible reaction mechanism for the formation of the ZMP imidazole was also reported.