117600-56-3 Usage
Chemical structure
A heterocyclic compound with a triazolopyridine ring and phenyl groups attached to positions 1 and 3.
Molecular weight
Approximately 255.3 g/mol
Appearance
It is likely to be a solid or crystalline substance, although the exact appearance may vary depending on the specific conditions.
Solubility
The solubility of 1,2,4-Triazolo[4,3-a]pyridine, 1,8a-dihydro-1,3-diphenyl- is not explicitly mentioned, but it may be soluble in organic solvents such as dimethyl sulfoxide (DMSO) or methanol, which are commonly used in medicinal chemistry.
Medicinal chemistry application
Used in the synthesis and development of potential pharmaceutical agents.
Biological activities
Studied for its potential interactions with biological targets such as enzymes, receptors, and proteins.
Potential medical applications
Investigated for its potential use in the treatment of various medical conditions.
Versatility
Shows promise as a versatile building block for the development of novel drug candidates.
Pharmaceutical industry
Has potential applications in the pharmaceutical industry due to its unique structure and potential biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 117600-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,0 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117600-56:
(8*1)+(7*1)+(6*7)+(5*6)+(4*0)+(3*0)+(2*5)+(1*6)=103
103 % 10 = 3
So 117600-56-3 is a valid CAS Registry Number.
117600-56-3Relevant academic research and scientific papers
Reactions of 1,3-Dipoles with Heterocycles, 8. - Synthesis of 1,8a-Dihydrotriazolopyridines and Benzologues
Grubert, Lutz,Jugelt, Werner,Bress, Hans Joachim,Koeppel, Hubert,Strietzel, Ute,Dombrowski, Anke
, p. 885 - 894 (2007/10/02)
The C,N double bond of pyridine, quinoline and isoquinoline as heterodipolarophile react with diarylnitrilimines 2, generated in situ by dehydrohalogenation of N-phenylbenzhydrazonoyl chlorides 1, in a cycloaddition with complete regioselectivity.A facile
