Product Name:2,2'-Dinitrobibenzyl

IUPAC Name:1-nitro-2-[2-(2-nitrophenyl)ethyl]benzene

CAS:16968-19-7
Molecular Formula:C14H12N2O4
Purity:95%
Catalog Number:CM250224
Molecular Weight:272.26

Packing Unit Available Stock Price($) Quantity
CM250224-500g in stock ƿůŗ
CM250224-1000g in stock ȃIJľ

For R&D use only.

Inquiry Form

   refresh    

Product Details

CAS NO:16968-19-7
Molecular Formula:C14H12N2O4
Melting Point:-
Smiles Code:O=[N+](C1=CC=CC=C1CCC2=CC=CC=C2[N+]([O-])=O)[O-]
Density:
Catalog Number:CM250224
Molecular Weight:272.26
Boiling Point:391.6°C at 760 mmHg
MDL No:MFCD00024296
Storage:Store at room temperature.

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Column Infos

Related Products



Product Other Information

Product Overview 2,2'-Dinitrobibenzyl (DNB) is an organic compound that belongs to the class of nitroaromatics. It is an aromatic compound, meaning that it contains a benzene ring with a nitro group attached to it. DNB is a yellow-orange crystalline solid at room temperature and has a molecular weight of 213.14 g/mol. It has a melting point of 99-100 °C and a boiling point of 349 °C. DNB is soluble in organic solvents such as ethanol and acetone, but is insoluble in water.
Synthesis and Application 2,2'-Dinitrobibenzyl is typically synthesized through the reaction of 2,2'-dinitrochlorobenzene with sodium borohydride. This reaction takes place in an aqueous solution of sodium hydroxide and results in the formation of the desired product, 2,2'-Dinitrobibenzyl. The reaction is shown below: 2,2'-Dinitrochlorobenzene + NaBH4 → 2,2'-Dinitrobibenzyl + NaCl 2,2'-Dinitrobibenzyl has been used extensively in scientific research for a variety of applications. It has been used to study the effects of nitroaromatics on the environment, as well as to study the biochemical and physiological effects of these compounds on living organisms. 2,2'-Dinitrobibenzyl has also been used to study the mechanism of action of certain drugs and to evaluate the potential toxicity of these drugs. In addition, 2,2'-Dinitrobibenzyl has been used in the synthesis of other compounds, such as nitrofurans, and in the preparation of certain organic solvents.
Future Directions There are several potential future directions for research involving 2,2'-Dinitrobibenzyl. One potential direction is to further explore the biochemical and physiological effects of 2,2'-Dinitrobibenzyl on living organisms. Additionally, research could be conducted to further elucidate the mechanism of action of 2,2'-Dinitrobibenzyl and to develop new applications for the compound. Finally, research could be conducted to develop new synthetic methods for the production of 2,2'-Dinitrobibenzyl and to explore the potential toxicity of the compound.