177775-87-0 Usage
Uses
Used in Organic Synthesis:
9-Benzoyl-3-bromo-9H-carbazole serves as a valuable building block in organic synthesis, contributing to the creation of complex organic molecules and compounds.
Used in Materials Science:
In the field of materials science, 9-Benzoyl-3-bromo-9H-carbazole is utilized for the modification of polymers and the development of organic optoelectronic devices. The benzoyl group enhances its applicability in these areas.
Used in Pharmaceutical Development:
The unique molecular structure and properties of 9-Benzoyl-3-bromo-9H-carbazole make it a promising candidate for the development of novel drugs and pharmaceuticals, indicating its potential in medicinal chemistry.
Used in Further Functionalization Reactions:
The presence of the bromine atom in 9-Benzoyl-3-bromo-9H-carbazole allows for further functionalization reactions, expanding its utility in chemical research and compound modification.
Check Digit Verification of cas no
The CAS Registry Mumber 177775-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,7,7 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 177775-87:
(8*1)+(7*7)+(6*7)+(5*7)+(4*7)+(3*5)+(2*8)+(1*7)=200
200 % 10 = 0
So 177775-87-0 is a valid CAS Registry Number.
177775-87-0Relevant articles and documents
Electrochemical Synthesis of Carbazoles by Dehydrogenative Coupling Reaction
Kehl, Anton,Schupp, Niclas,Breising, Valentina M.,Schollmeyer, Dieter,Waldvogel, Siegfried R.
, p. 15847 - 15851 (2020/11/02)
A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N-protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.
TFAA/H3PO4 mediated unprecedented N-acylation of carbazoles leading to small molecules possessing anti-proliferative activities against cancer cells
Kolli, Sunder Kumar,Prasad, Bagineni,Babu, P. Vijaya,Ashfaq, Mohd Ashraf,Ehtesham, Nasreen Z.,Raju, R. Ramesh,Pal, Manojit
supporting information, p. 6080 - 6084 (2014/08/05)
For the first time TFAA/H3PO4 has facilitated the direct and metal-free N-acylation of carbazoles leading to a number of N-acylated derivatives. Several of these compounds were found to be promising when tested for their anti-proliferative properties against oral cancer cell lines. This journal is the Partner Organisations 2014.
