116072-25-4 Usage
Ethyl ester derivative
The molecule has an ethyl ester functional group (-COOCH3) attached to the pyrazole ring, which influences its reactivity and properties.
Heterocyclic compound
The compound contains a pyrazole ring, which is a five-membered ring with three carbon atoms and two nitrogen atoms.
Pyrazole ring
The central feature of the compound is the pyrazole ring, which contributes to its unique chemical properties.
1,3,4-Triphenyl substitution
The pyrazole ring has three phenyl groups (-C6H5) attached to it at positions 1, 3, and 4, which may affect its solubility, stability, and reactivity.
transconfiguration
The substituents on the pyrazole ring are in a transconfiguration, meaning they are positioned opposite each other, which influences the compound's geometry and properties.
Potential applications
This chemical may have potential uses in pharmaceutical and agricultural industries, as well as in the synthesis of other organic compounds.
Further research needed
More research and testing are required to determine the specific properties and potential uses of 1H-Pyrazole-5-carboxylic acid, 4,5-dihydro-1,3,4-triphenyl-, ethyl ester,
trans-.
Check Digit Verification of cas no
The CAS Registry Mumber 116072-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116072-25:
(8*1)+(7*1)+(6*6)+(5*0)+(4*7)+(3*2)+(2*2)+(1*5)=94
94 % 10 = 4
So 116072-25-4 is a valid CAS Registry Number.
116072-25-4Relevant academic research and scientific papers
Porous calcium hydroxyapatite as an efficient catalyst for synthesis of pyrazolines via 1,3-dipolar cycoloaddition under solvent-free microwave irradiation
Atir,Mallouk,Bougrin,Soufiaoui,Laghzizil
, p. 111 - 120 (2007/10/03)
Adsorbed on porous calcium hydroxyapatite, 1,3-dipolar cycloaddition of diphenylnitrilimine on olefins is readily catalyzed under solvent-free microwaves irradiation. The pyrazolines are obtained in few minutes with high yields. Specific surface of porous
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
Dihalogentriphenylphosphoranes in Heterocyclic Synthesis; 15. A Simple One-Pot-Procedure for the Generation of Nitrilimines with the Aid of Dihalogentriphenylphosphoranes: 1,3-Dipolar Cycloadditions and 1,5-Electrocyclizations
Wamhoff, Heinrich,Zahran, Magdy
, p. 876 - 879 (2007/10/02)
A simple and versatile one-pot procedure for the in situ generation of nitrilimines from N-acyl hydrazines is described. 1,3-Dipolar cycloadditions and 1,5-electrocyclic ring closures are carried out.Unsymmetrically substituted dipolarophiles show typical
