151055-85-5 Usage
Uses
Used in Pharmaceutical Research:
2-[3-(1H-imidazol-1-yl)phenyl]-1,3-dioxolane is utilized as a potential drug candidate for the development of new medications. Its imidazole ring allows for interactions with various biological targets, which is crucial for the creation of effective pharmaceuticals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-[3-(1H-imidazol-1-yl)phenyl]-1,3-dioxolane serves as a valuable compound for designing and synthesizing novel therapeutic agents. The structural components of the compound, including the dioxolane ring, can be manipulated to optimize its pharmacological properties and efficacy.
Used in Drug Development:
2-[3-(1H-imidazol-1-yl)phenyl]-1,3-dioxolane is employed in drug development processes to create new therapeutic agents. Its unique structure and the ability of the imidazole ring to bind with biological targets make it a promising candidate for further research and development into potential treatments for various diseases and conditions.
Used in Biological Target Interaction:
2-[3-(1H-imidazol-1-yl)phenyl]-1,3-dioxolane is used in the study and interaction with biological targets, which is essential for understanding its potential therapeutic effects and for guiding the design of new drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 151055-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,5 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 151055-85:
(8*1)+(7*5)+(6*1)+(5*0)+(4*5)+(3*5)+(2*8)+(1*5)=105
105 % 10 = 5
So 151055-85-5 is a valid CAS Registry Number.
151055-85-5Relevant academic research and scientific papers
Ultrafast singlet - singlet energy transfer in self-assembled via metal - ligand axial coordination of free-base porphyrin - zinc phthalocyanine and free-base porphyrin - zinc naphthalocyanine Dyads
Maligaspe, Eranda,Kumpulainen, Tatu,Lemmetyinen, Helge,Tkachenko, Nikolai V.,Subbaiyan, Navaneetha K.,Zandler, Melvin E.,D'Souza, Francis
experimental part, p. 268 - 277 (2010/05/11)
Singlet - singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H2PIm, to either zinc phthalocyanine, ZnPc, or zinc nap
Imidazol-1-yl and Pyridin-3-yl Derivatives of 4-Phenyl-1,4-dihydropyridines Combining Ca2+ Antagonism and Thromboxane A2 Synthase Inhibition
Cozzi, Paolo,Carganico, Germano,Fusar, Domenico,Grossoni, Mauro,Menichincheri, Maria,et al.
, p. 2964 - 2972 (2007/10/02)
A series of derivatives of 4-phenyl-1,4-dihydropyridine bearing imidazol-1-yl or pyridin-3-yl moieties on the phenyl ring were synthesized with the aim of combining Ca2+ antagonism and thromboxane A2 (Tx A2) synthase inhib
