952183-23-2 Usage
Type of compound
Heterocyclic compound
Triazole ring
A five-membered ring with three nitrogen atoms and two carbon atoms
Hydroxymethyl group
A hydroxyl (-OH) group attached to a methyl (-CH3) group
Hydroxymethyl group
Involved in various chemical reactions, making the compound a versatile building block for the synthesis of other complex organic molecules
Fluorobenzyl group
A benzyl group (C6H5-CH2-) with a fluorine atom attached to the benzene ring
Fluorobenzyl group
Imparts specific chemical and biological properties to the molecule
Potential applications
Medicinal chemistry and drug discovery
Biological activities
Antimicrobial, antiviral, and anticancer properties
Ongoing research
Further research and development into the properties and potential applications of 1-(3-Fluorobenzyl)-4-(hydroxymethyl)-1H-1,2,3-triazole are ongoing.
Check Digit Verification of cas no
The CAS Registry Mumber 952183-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,1,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 952183-23:
(8*9)+(7*5)+(6*2)+(5*1)+(4*8)+(3*3)+(2*2)+(1*3)=172
172 % 10 = 2
So 952183-23-2 is a valid CAS Registry Number.
952183-23-2Relevant academic research and scientific papers
Anti-Lung Cancer Activities of 1,2,3-Triazole Curcumin Derivatives via Regulation of the MAPK/NF-κB/STAT3 Signaling Pathways
Zhi, Tai Xin,Liu, Kai Qiang,Cai, Kun Yi,Zhao, Yu Chao,Li, Zhen Wang,Wang, Xin,He, Xin Hua,Sun, Xian Yu
, (2021/12/01)
In this study, a series of curcumin derivatives containing 1,2,3-triazole were designed and synthesized, and their inhibitory activities against the proliferation of lung cancer cells were studied. Compound 5 k (3,4-dichlorobenzyltriazole methyl curcumin)
New mono- and bidentate P-ligands using one-pot click-chemistry: Synthesis and application in Rh-catalyzed hydroformylation
Dubrovina, Natalia V.,Domke, Lutz,Shuklov, Ivan A.,Spannenberg, Anke,Franke, Robert,Villinger, Alexander,B?rner, Armin
, p. 8809 - 8817 (2013/09/23)
Three families of new phosphorus ligands have been prepared using the click-chemistry approach proceeding in only two steps and without intermediate P-protection. The methodology allows the high yield production of mono- and bidentate P-ligands, bearing at least one P-O bond. The ligands were tested in the Rh-catalyzed hydroformylation of 1-octene.
