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3H-Indolizino[8,7-b]indol-3-one, 1,2,5,6,11,11b-hexahydro-11b-phenyl- is a complex organic compound with the molecular formula C20H18N2O. It is a derivative of indolizine, a heterocyclic compound with a fused indole ring. This specific compound features a hexahydro structure, indicating the presence of six hydrogen atoms in a cyclic structure, and an 11b-phenyl group, which is a phenyl ring attached to the molecule at the 11b position. The compound is characterized by its unique molecular structure and potential applications in various chemical and pharmaceutical research areas.

741-25-3

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741-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741-25-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,4 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 741-25:
(5*7)+(4*4)+(3*1)+(2*2)+(1*5)=63
63 % 10 = 3
So 741-25-3 is a valid CAS Registry Number.

741-25-3Relevant academic research and scientific papers

Racemic and diastereoselective construction of indole alkaloids under solvent- and catalyst-free microwave-assisted Pictet-Spengler condensation

Jida, Mouhamad,Soueidan, Olivier-Mohamad,Deprez, Benoit,Laconde, Guillaume,Deprez-Poulain, Rebecca

supporting information; experimental part, p. 909 - 911 (2012/06/18)

An environment-friendly high-yielding method for the racemic and asymmetric diastereoselective preparation of indole alkaloids via Pictet-Spengler reaction is reported. The reaction proceeds with short reaction times under solvent-free and microwave-irrad

Dopamine/serotonin receptor ligands. 10: SAR studies on azecine-type dopamine receptor ligands by functional screening at human cloned D1, D2L, and D5 receptors with a microplate reader based calcium assay lead to a novel potent D1/D5 selective antagonist

Hoefgen, Barbara,Decker, Michael,Mohr, Patrick,Schramm, Astrid M.,Rostom, Sherif A. F.,El-Subbagh, Hussein,Schweikert, Peter M.,Rudolf, Dirk R.,Kassack, Matthias U.,Lehmann, Jochen

, p. 760 - 769 (2007/10/03)

On the basis of the benz[d]indolo[2,3-g]azecine derivative 1 (LE300), structure-activity relations were investigated in order to identify the pharmacophore in this new class of ligands. Various structural modifications were performed and the inhibitory activities at human cloned D1, D2L, and D5 receptors were measured by using a simple fluorescence microplate reader based calcium assay. Subsequently, the affinities of active compounds were estimated by radioligand binding experiments, Deleting one of the aromatic rings as well as replacing it by a phenyl moiety abolishes the inhibitory activities almost completely. Contraction of the 10-membered central ring decreases them significantly. The replacement of indole by thiophene or N-methylpyrrole reduces the inhibitory activity, whereas replacing the indole by benzene increases it. Finally, the hydroxylated dibenz[d,g]azecine derivative 11d (LE404) was found to be more active than the lead 1 in the functional calcium assay as well as in radioligand displacement experiments.

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