108664-39-7 Usage
Chemical structure
1-biphenyl-4-yl-2-(1H-1,2,4-triazol-1-ylmethyl)prop-2-en-1-one is an organic compound with a complex chemical structure, consisting of a biphenyl group attached to a propenone group through a 1,2,4-triazole ring.
Application in medicinal chemistry
It is commonly used in medicinal chemistry as a building block for the synthesis of various pharmaceuticals and bioactive molecules.
Potential antifungal and antimicrobial properties
The compound has been studied for its potential antifungal and antimicrobial properties.
Bioactivity of the triazole moiety
The triazole moiety in its structure is known for its bioactivity.
Structural diversity provided by the biphenyl group
The biphenyl group provides additional structural diversity for the design of novel drugs.
Versatility
1-biphenyl-4-yl-2-(1H-1,2,4-triazol-1-ylmethyl)prop-2-en-1-one is a versatile chemical.
Potential applications
It has potential applications in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 108664-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108664-39:
(8*1)+(7*0)+(6*8)+(5*6)+(4*6)+(3*4)+(2*3)+(1*9)=137
137 % 10 = 7
So 108664-39-7 is a valid CAS Registry Number.
108664-39-7Relevant articles and documents
Synthesis and Antifungal Activity of a Series of Novel 1,2-Disubstituted Propenones
Ogata, Masaru,Matsumoto, Hiroshi,Kida, Shiro,Shimizu, Sumio,Tawara, Katsuya,Kawamura, Yoshimi
, p. 1497 - 1502 (2007/10/02)
To find an antifungal agent other than those of the imidazole and triazole series, a new class of 1,2-disubstituted propenones I and II was prepared and tested for antifungal activity.Comparison of the structure-activity relationships showed that the conjugated structure of carbonyl and exomethylene groups in I and II plays an important role in potent antifungal acivity.However, it is noteworthy that compounds 53, 54, and 56, which have a hydroxymethyl or methoxymethyl group instead of an exo-methylene group in I, also showed potent activity.Although many compounds exhibited strong antifungal activity in vitro, none showed activity in vivo of oral efficacy against subacute systemic candidiasis in mice. '