177775-87-0 Usage
General Description
9-Benzoyl-3-bromo-9H-carbazole is a chemical compound that consists of a carbazole core with a benzoyl group and a bromine atom attached to it. It is commonly used as a building block in organic synthesis and has several potential applications in the field of materials science. The presence of the benzoyl group makes this compound useful for the modification of polymers and the development of organic optoelectronic devices, while the bromine atom can facilitate further functionalization reactions. Additionally, its unique molecular structure and properties make it a valuable candidate for the development of novel drugs and pharmaceuticals. Overall, 9-Benzoyl-3-bromo-9H-carbazole is a versatile and valuable chemical that has numerous potential applications across different scientific disciplines.
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.
