19279-70-0 Usage
Organic compound
It is a carbon-based compound, as most of its structure is derived from carbon atoms and various functional groups.
Derivative of isoindole
The compound is derived from the heterocyclic compound isoindole, which is a fused bicyclic structure containing both carbon and nitrogen atoms.
Heterocyclic compound
The presence of nitrogen in its structure makes it a heterocyclic compound, which is a compound containing a ring of atoms with at least one non-carbon atom.
Benzylideneamino group
The compound contains a benzylideneamino group (-NH-C6H5), which is an aromatic amine group connected to a phenyl ring through a carbon atom.
Potential biological activities
The compound has been studied for its possible antimicrobial and anticancer properties, indicating its potential as a therapeutic agent.
Organic synthesis
2-[(4-methoxybenzylidene)amino]-1H-isoindole-1,3(2H)-dione has been explored for its potential use in organic synthesis, making it a versatile building block for creating new compounds.
Fluorescent probe
The compound has been researched as a potential fluorescent probe, which could be used to study biological processes or detect specific molecules in a sample.
Pharmaceutical and industrial applications
Due to its unique chemical structure and potential biological activities, the compound may have various applications in the pharmaceutical industry and other industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 19279-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19279-70:
(7*1)+(6*9)+(5*2)+(4*7)+(3*9)+(2*7)+(1*0)=140
140 % 10 = 0
So 19279-70-0 is a valid CAS Registry Number.
19279-70-0Relevant articles and documents
Extending the Scope of the B(C6F5)3-Catalyzed C=N Bond Reduction: Hydrogenation of Oxime Ethers and Hydrazones
Mohr, Jens,Porwal, Digvijay,Chatterjee, Indranil,Oestreich, Martin
supporting information, p. 17583 - 17586 (2015/12/05)
The B(C6F5)3-catalyzed hydrogenation is applied to aldoxime triisopropylsilyl ethers and hydrazones bearing an easily removable phthaloyl protective group. The C=N reduction of aldehyde-derived substrates (oxime ethers and hydrazones) is enabled by using 1,4-dioxane as the solvent known to participate as the Lewis-basic component in FLP-type heterolytic dihydrogen splitting. More basic ketone-derived hydrazones act as Lewis bases themselves in the FLP-type dihydrogen activation and are therefore successfully hydrogenated in nondonating toluene. The difference in reactivity between aldehyde- and ketone-derived substrates is also reflected in the required catalyst loading and dihydrogen pressure.