2362-57-4 Usage
Description
(6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one is a hydrazine derivative featuring a cyclohexenone structure, also known as 6-phenylhydrazinylidenecyclohexa-2,4-dien-1-one. The (6Z) in its name signifies a cis geometry at the double bond between the sixth and seventh carbon atoms. (6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one is recognized for its potential applications in organic synthesis and medicinal chemistry, attributed to its functional hydrazine and cyclohexenone groups that can engage in diverse chemical reactions and interactions with biological targets. Furthermore, its aromatic phenyl group may enhance its chemical and biological properties.
Uses
Used in Organic Synthesis:
(6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one is used as a synthetic intermediate for the creation of various complex organic molecules. Its reactive functional groups allow for a wide range of chemical reactions, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one is utilized as a starting material for the development of new drugs. Its ability to interact with biological targets, such as enzymes and receptors, makes it a promising candidate for the treatment of various diseases. (6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one's hydrazine and cyclohexenone functional groups can be further modified to improve its pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Pharmaceutical Industry:
(6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one is used as a key component in the formulation of novel pharmaceuticals. Its unique structure and functional groups enable the design of drugs with improved therapeutic profiles, targeting a range of medical conditions, including but not limited to, cancer, inflammation, and infectious diseases.
Used in Chemical Research:
(6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one is also employed as a research tool in chemical laboratories to study the reactivity and properties of hydrazine and cyclohexenone functional groups. Understanding the behavior of (6Z)-6-(phenylhydrazono)cyclohexa-2,4-dien-1-one in various chemical reactions can provide valuable insights into the development of new synthetic methods and the design of innovative molecules with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2362-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2362-57:
(6*2)+(5*3)+(4*6)+(3*2)+(2*5)+(1*7)=74
74 % 10 = 4
So 2362-57-4 is a valid CAS Registry Number.
2362-57-4Relevant articles and documents
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Buncel,Lawton
, p. 862,865 (1965)
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Palladium catalyzed Csp2-H activation for direct aryl hydroxylation: The unprecedented role of 1,4-dioxane as a source of hydroxyl radicals
Seth, Kapileswar,Nautiyal, Manesh,Purohit, Priyank,Parikh, Naisargee,Chakraborti, Asit K.
supporting information, p. 191 - 194 (2015/01/09)
A novel strategy for direct aryl hydroxylation via Pd-catalysed Csp2-H activation through an unprecedented hydroxyl radical transfer from 1,4-dioxane, used as a solvent, is reported with bio relevant and sterically hindered heterocycles and various acyclic functionalities as versatile directing groups.
Photochemical Behavior of 1,3-Diaryltriazene 1-Oxides
El-Din, Ahmed Moukhtar Nour,Mohamed, Shaaban Kamel,Doepp, Dietrich
, p. 131 - 135 (2007/10/03)
Photolysis of the 1,3-dipolar unsymmetrical 1,3-triazene 1-oxides in aromatic and nonaromatic solvents led to their decomposition. 2-Hydroxyazobenzene, mono- and disubstituted biaryls were produced.
