15096-05-6 Usage
Description
(6Z)-6-[(4-methoxyphenyl)hydrazono]-4-methylcyclohexa-2,4-dien-1-one is an organic compound belonging to the hydrazone derivative class, characterized by a carbon-nitrogen double bond linked to an imine group. It features a cyclohexadienone ring structure with a methyl and methoxyphenyl group attached, which may contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(6Z)-6-[(4-methoxyphenyl)hydrazono]-4-methylcyclohexa-2,4-dien-1-one is used as a potential pharmaceutical compound for its unique structure and properties. (6Z)-6-[(4-methoxyphenyl)hydrazono]-4-methylcyclohexa-2,4-dien-1-one's hydrazone nature and cyclohexadienone ring may offer opportunities for the development of new drugs, targeting specific diseases or conditions.
Used in Agrochemical Industry:
In the agrochemical industry, (6Z)-6-[(4-methoxyphenyl)hydrazono]-4-methylcyclohexa-2,4-dien-1-one may be utilized as a starting material or intermediate for the synthesis of novel agrochemicals, such as pesticides or herbicides, due to its specific structural features.
Used in Materials Science:
(6Z)-6-[(4-methoxyphenyl)hydrazono]-4-methylcyclohexa-2,4-dien-1-one's unique structure and properties could also make it a candidate for applications in materials science. It may be investigated for its potential to contribute to the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 15096-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,9 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15096-05:
(7*1)+(6*5)+(5*0)+(4*9)+(3*6)+(2*0)+(1*5)=96
96 % 10 = 6
So 15096-05-6 is a valid CAS Registry Number.
15096-05-6Relevant articles and documents
A Chemoselective Rapid Azo-Coupling Reaction (CRACR) for Unclickable Bioconjugation
Addy, Partha Sarathi,Erickson, Sarah B.,Italia, James S.,Chatterjee, Abhishek
supporting information, p. 11670 - 11673 (2017/09/07)
Chemoselective modification of complex biomolecules has become a cornerstone of chemical biology. Despite the exciting developments of the past two decades, the demand for new chemoselective reactions with unique abilities, and those compatible with existing chemistries for concurrent multisite-directed labeling, remains high. Here we show that 5-hydroxyindoles exhibit remarkably high reactivity toward aromatic diazonium ions and this reaction can be used to chemoselectively label proteins. We have previously genetically encoded the noncanonical amino acid 5-hydroxytryptophan in both E. coli and eukaryotes, enabling efficient site-specific incorporation of 5-hydroxyindole into virtually any protein. The 5-hydroxytryptophan residue was shown to allow rapid, chemoselective protein modification using the azo-coupling reaction, and the utility of this bioconjugation strategy was further illustrated by generating a functional antibody-fluorophore conjugate. Although the resulting azo-linkage is otherwise stable, we show that it can be efficiently cleaved upon treatment with dithionite. Our work establishes a unique chemoselective "unclickable" bioconjugation strategy to site-specifically modify proteins expressed in both bacteria and eukaryotes.
REACTIVITY AND MECHANISM OF THE ANTITUMOR ACTION OF TRIAZENES. II. INTERACTION OF AROMATIC DIAZO-DERIVATIVES WITH A MODEL OF PHENOL-TYPE NUCLEOPHILIC SITES OF THE CELL MEMBRANES
Nifontov, V. I.,Bel'skaya, N. P.,Shishkina, V. I.,Chernov, V. A.,Ershova, Yu. A.,et al.
, p. 162 - 166 (2007/10/02)
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