Product Name:Ethyl 4-(2-hydroxy-5-methyl-3-nitrophenyl)-2,4-dioxobutanoate

IUPAC Name:ethyl 4-(2-hydroxy-5-methyl-3-nitrophenyl)-2,4-dioxobutanoate

CAS:859843-60-0
Molecular Formula:C13H13NO7
Purity:95%
Catalog Number:CM309694
Molecular Weight:295.25

Packing Unit Available Stock Price($) Quantity

For R&D use only.

Inquiry Form

   refresh    

Product Details

CAS NO:859843-60-0
Molecular Formula:C13H13NO7
Melting Point:-
Smiles Code:O=C(OCC)C(CC(C1=CC(C)=CC([N+]([O-])=O)=C1O)=O)=O
Density:
Catalog Number:CM309694
Molecular Weight:295.25
Boiling Point:
MDL No:
Storage:Store at 2-8°C.

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.

Related Products



Product Other Information

Product Overview Ethyl 4-(2-hydroxy-5-methyl-3-nitrophenyl)-2,4-dioxobutanoate, more commonly known as ethyl 4-nitrobenzoate, is a nitrobenzoic acid ester that is used in a variety of scientific research applications. It is a colorless solid that is soluble in organic solvents and has a melting point of approximately 118°C. This compound has a wide range of applications in biochemical, physiological, and medicinal research.
Synthesis and Application Ethyl 4-nitrobenzoate can be synthesized through a two-step process. The first step involves the reaction of 4-nitrobenzoic acid with ethanol in the presence of a strong base such as sodium hydroxide. The reaction produces ethyl 4-nitrobenzoate and sodium 4-nitrobenzoate. The second step involves the removal of the sodium 4-nitrobenzoate by-product through a simple filtration process. Ethyl 4-nitrobenzoate has a wide range of applications in scientific research. It is used in the synthesis of various compounds, such as nitroalkanes and nitroaromatics. It is also used as a reagent in the synthesis of pharmaceuticals and other organic compounds. Additionally, ethyl 4-nitrobenzoate can be used as a fluorescent probe for the detection of carboxylic acids and amines.
Future Directions In the future, ethyl 4-nitrobenzoate could be used to develop new fluorescent probes for the detection of other compounds, such as proteins and nucleic acids. Additionally, it could be used in the synthesis of new drugs and other compounds with potential therapeutic applications. Finally, further research could be done to explore the biochemical and physiological effects of ethyl 4-nitrobenzoate on living organisms.