1248256-35-0 Usage
Triazole derivative
A class of heterocyclic compounds containing a five-membered ring with three nitrogen atoms, which provides a versatile structure for various chemical reactions and applications.
Building block in medicinal chemistry
Commonly used in drug discovery 1-Phenyl-4-(bromomethyl)-1,2,3-triazole serves as a starting point for the synthesis of biologically active molecules, contributing to the development of new drugs.
Bromomethyl group
A key functional group the presence of the bromomethyl group makes the compound suitable for use as a linker in the synthesis of various bioactive compounds, allowing for the attachment of different molecules to create new compounds with specific properties.
Potential pharmacological applications
Antitumor and antiviral properties the compound has been studied for its possible use in treating cancer and viral infections, making it a valuable target for further research in these areas.
Interest to researchers
Organic chemistry and pharmaceutical science due to its versatile nature and potential applications in drug development, 1-Phenyl-4-(bromomethyl)-1,2,3-triazole is of great interest to researchers working in both organic chemistry and pharmaceutical science fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1248256-35-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,2,5 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1248256-35:
(9*1)+(8*2)+(7*4)+(6*8)+(5*2)+(4*5)+(3*6)+(2*3)+(1*5)=160
160 % 10 = 0
So 1248256-35-0 is a valid CAS Registry Number.
1248256-35-0Relevant articles and documents
Key Non-Metal Ingredients for Cu-catalyzed “Click” Reactions in Glycerol: Nanoparticles as Efficient Forwarders
Rodríguez-Rodríguez, Marta,Llanes, Patricia,Pradel, Christian,Pericàs, Miquel A.,Gómez, Montserrat
, p. 18247 - 18253 (2016/12/16)
The effect of long-alkyl-chain amines in CuI-assisted azide–alkyne cycloadditions of terminal alkynes with organic azides in glycerol and other environmentally benign solvents (water, ethanol) has been examined. The presence of these additives favors the
