4880-96-0 Usage
Uses
Used in Organic Synthesis:
1-(2-bromo-1-phenylethylidene)-2-(2,4-dinitrophenyl)hydrazine is used as an intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable compound in the synthesis of pharmaceuticals and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(2-bromo-1-phenylethylidene)-2-(2,4-dinitrophenyl)hydrazine may be utilized as a building block for the development of new drugs. Its structural features could potentially be exploited to design molecules with specific biological activities, targeting various diseases and medical conditions.
Used as a Chelating Agent:
Due to the presence of nitrogen atoms in its structure, 1-(2-bromo-1-phenylethylidene)-2-(2,4-dinitrophenyl)hydrazine may have potential use as a chelating agent. It could be employed to form stable complexes with metal ions, which can be useful in various industrial applications, including the removal of metal ions from waste streams or the stabilization of metal ions in chemical processes.
Used in Coordination Chemistry:
In coordination chemistry, 1-(2-bromo-1-phenylethylidene)-2-(2,4-dinitrophenyl)hydrazine may serve as a ligand, bonding to metal ions to form coordination complexes. These complexes can have a range of applications, from catalysts in chemical reactions to materials with unique electronic or magnetic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 4880-96-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4880-96:
(6*4)+(5*8)+(4*8)+(3*0)+(2*9)+(1*6)=120
120 % 10 = 0
So 4880-96-0 is a valid CAS Registry Number.
4880-96-0Relevant academic research and scientific papers
Addition of malonic esters to azoalkenes generated in situ from α-bromo- and α-chlorohydrazones
Kokuev, Aleksandr O.,Ioffe, Sema L.,Sukhorukov, Alexey Yu.
supporting information, (2021/10/04)
Michael addition of malonic esters to azoalkenes generated in situ from α-bromo- and α-chlorohydrazones was accomplished. Both aliphatic and aromatic substrates bearing different functional groups are tolerated. The use of a strong base (sodium hydride) for generation of azoalkenes and deprotonation of malonate was found to be essential for a successful coupling. Synthetic potential of the obtained β-hydrazonoalkylmalonates was demonstrated by their smooth conversion into five- and six-membered N-heterocycles, functionalized hydrazides, 2-(2-oxo-2-arylethyl)malonates and 2-arylethylmalonates.
E/Z isomerism in monoalkylated derivatives of [Pt2(μ-S) 2(PPH3)4] containing 2,4-dinitrophenylhydrazone substituents
Ujam, Oguejiofo T.,Devoy, Sarah M.,Henderson, William,Wilkins, Alistair L.,Nicholson, Brian K.
experimental part, p. 2782 - 2790 (2012/02/15)
Alkylation of [Pt2(μ-S)2(PPH3) 4] with 2,4-dinitrophenylhydrazone-functionalized alkylating agents XC6H4C{=NNHC6H3(NO2) 2}CH2Br (X = H
