6192-43-4 Usage
Derivative of phenoxazine
Yes
A derivative is a compound that is structurally related to another compound, in this case, phenoxazine.
Contains an acetyl group
Yes
An acetyl group is a functional group with the formula CH3CO-, which is attached to the phenoxazine molecule.
Used in organic synthesis
Yes
Organic synthesis is the process of creating organic compounds by forming or breaking chemical bonds.
Used in pharmaceutical research
Yes
Pharmaceutical research involves the study and development of drugs and medications.
Building block for pharmaceuticals
Yes
It can be used as a starting material or intermediate in the synthesis of various pharmaceuticals.
Building block for dyes
Yes
It can also be used in the synthesis of dyes, which are substances that impart color to materials.
Potential applications in materials science
Yes
Materials science is the study and development of materials with specific properties, such as organic electronic devices.
Range of potential uses
Various industries and research fields
The compound has a wide range of potential applications, making it valuable in different sectors.
Structure
10H-Phenoxazine with an acetyl group attached
The structure of the compound consists of a phenoxazine ring with an acetyl group (CH3CO-) attached to it.
Check Digit Verification of cas no
The CAS Registry Mumber 6192-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6192-43:
(6*6)+(5*1)+(4*9)+(3*2)+(2*4)+(1*3)=94
94 % 10 = 4
So 6192-43-4 is a valid CAS Registry Number.
6192-43-4Relevant articles and documents
Microwave assisted rapid synthesis of phenoxazines and benzopyridoxazines
Anchan, Kavitha,Puttappa, Nagaswarupa H.,Poongavanam, Baburajan,Sarkar, Sujit Kumar
, p. 635 - 646 (2020/11/27)
A facile protocol for the synthesis of phenoxazines and benzopyridoxazines by Smiles rearrangement have been demonstrated in short reaction time under microwave irradiation. The control experiments suggest that a reaction proceeds through Smiles rearrangement followed SNAr ring closure by in situ cascade process. In our present work, both the electron donating and electron withdrawing groups were tolerant and provided a corresponding phenoxazine/benzopyridoxazine in good to moderate yields.
