152665-33-3 Usage
Uses
Used in Pharmaceutical Applications:
DMTCC is utilized as a pharmaceutical agent for its antimicrobial, antifungal, and antiproliferative properties, offering potential treatments for various infections and diseases.
Used in Coordination Chemistry:
In the field of coordination chemistry, DMTCC serves as a ligand, enabling the formation of metal complexes that can have specialized applications in areas such as catalysis and materials science.
Used in Biological Studies:
DMTCC is employed as a photoaffinity label in biological research, providing a tool for investigating the interactions of biomolecules with high specificity and sensitivity.
Used in Antimicrobial Applications:
DMTCC is used as an antimicrobial agent, effective against a range of microorganisms, offering a potential solution for combating microbial infections.
Used in Antifungal Applications:
2,6-dimethyl-4-(2-methyl-1H-tetrazol-5-ylidene)cyclohexa-2,5-dien-1-on e is applied as an antifungal agent, useful in treating fungal infections and controlling the growth of fungi in various settings.
Used in Antiproliferative Applications:
DMTCC is utilized in antiproliferative applications, particularly in the study and treatment of conditions characterized by uncontrolled cell growth, such as cancer.
Each of these applications leverages the unique properties of DMTCC, demonstrating its versatility and potential impact across different scientific and industrial areas.
Check Digit Verification of cas no
The CAS Registry Mumber 152665-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,6,6 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152665-33:
(8*1)+(7*5)+(6*2)+(5*6)+(4*6)+(3*5)+(2*3)+(1*3)=133
133 % 10 = 3
So 152665-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N4O/c1-6-4-8(5-7(2)9(6)15)10-11-13-14(3)12-10/h4-5,12H,1-3H3
152665-33-3Relevant academic research and scientific papers
Phenoxy- and phenoxyalkyl-piperidines as antiviral agents
-
, (2008/06/13)
Compounds of the formula STR1 wherein R1 is selected from STR2 Y is a bond or lower alkylene; R2 and R3 are independently hydrogen, lower-alkyl or halogen; R4 is STR3 R5 is hydrogen, lower-alkyl or halogen; R6 is hydrogen, lower-alkyl or halogen; R7 is hydrogen or lower-alkyl; R8 is hydrogen, lower-alkyl, or trifluoromethyl; R9 is lower-alkyl; R10 is lower-alkyl, trifluoromethyl or difluoromethyl; or pharmaceutically acceptable acid addition salts thereof are useful as antiviral agents.
Antipicornavirus Activity of Tetrazole Analogues Related to Disoxaril
Diana, Guy D.,Cutcliffe, David,Volkots, Deborah L.,Mallamo, John P.,Bailey, Thomas R.,et al.
, p. 3240 - 3250 (2007/10/02)
A series of tetrazole analogues of Win 54954, a broad-spectrum antipicornavirus compound, has been synthesized to address the acid lability of the oxazoline ring of this series of compounds.The results of X-ray crystallography studies of several members o
