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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Furancarboxaldehyde,5-nitro-, 2-[(5-nitro-2-furanyl)methylene]hydrazone

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Chemical Name: 2-Furancarboxaldehyde,5-nitro-, 2-[(5-nitro-2-furanyl)methylene]hydrazone
CAS Number: 736-53-8
Product Number: AG00FG9H(AGN-PC-0U3J8E)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


5-Nitro-2-furaldehydeazine, also known as 5-nitrofuraldehyde hydrazone, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various organic molecules through diverse chemical transformations.One key application of 5-Nitro-2-furaldehydeazine is as a precursor in the synthesis of heterocyclic compounds. By undergoing condensation reactions with various carbonyl compounds or amines, this compound can be utilized to form complex heterocycles with diverse substitution patterns. These heterocyclic structures have demonstrated significant biological activities and are instrumental in the development of pharmaceuticals and agrochemicals.In addition, 5-Nitro-2-furaldehydeazine plays a crucial role in the synthesis of azo dyes. Through diazotization and coupling reactions, this compound can be involved in the construction of colorful azo compounds widely used in the textile and chemical industries. The presence of the nitro group in 5-Nitro-2-furaldehydeazine provides an essential electron-withdrawing capability, allowing for the formation of vibrant azo dyes with excellent color fastness properties.Moreover, this compound can participate in various functional group transformations, such as reduction, oxidation, and substitution reactions, enabling the development of a diverse array of chemical structures with tailored properties. Overall, the application of 5-Nitro-2-furaldehydeazine in chemical synthesis showcases its significance as a versatile intermediate for the preparation of valuable organic compounds with wide-ranging industrial applications.