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2H-Pyrrole, 5-[(4-chlorophenyl)methyl]-3,4-dihydro- is a chemical compound with the molecular formula C11H12ClN. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with two carbon atoms and two nitrogen atoms. In this specific compound, the pyrrole ring is substituted with a 4-chlorophenylmethyl group at the 5-position, and the molecule is in a 3,4-dihydro form, indicating the presence of two hydrogen atoms attached to the ring, which reduces the aromaticity. 2H-Pyrrole, 5-[(4-chlorophenyl)methyl]-3,4-dihydro- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in organic chemistry.

66162-25-2

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66162-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66162-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,6 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66162-25:
(7*6)+(6*6)+(5*1)+(4*6)+(3*2)+(2*2)+(1*5)=122
122 % 10 = 2
So 66162-25-2 is a valid CAS Registry Number.

66162-25-2Relevant academic research and scientific papers

FUSED PYRROLE COMPOUNDS, PHARMACEUTICAL AGENTS CONTAINING THE SAME, AND THE USE THEREOF

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Page 41; 42, (2010/02/04)

The present invention relates to fused pyrrole compounds of the formula 1. in which at least one of the radicals R1, R2, R3 is 4-sulphur-substituted phenyl. These compounds are in particular pyrrolizines, indolizines and heteroanalogues having selective inhibitory action on isoenzyme-2 of prostaglandin H synthase (COX-2). The invention also relates to pharmaceutical compositions which contain these compounds; and the use of these compounds for the treatment of disorders of the rheumatic type.

Cyclooxygenase-1/2 (COX-1/COX-2) and 5-lipoxygenase (5-LOX) inhibitors of the 6,7-diaryl-2,3-1H-dihydropyrrolizine type

Ulbrich, Holger,Fiebich, Bernd,Dannhardt, Gerd

, p. 953 - 959 (2007/10/03)

A series of 6,7-diaryl-2,3-1H-dihydropyrrolizines was prepared as COX-1/COX-2 and 5-LOX inhibitors. The inhibition of COX-1 was evaluated using intact bovine platelets as the enzyme source, whereas LPS-stimulated human monocytes served as the enzyme source for inducible COX-2. The determination of arachidonic metabolites was performed by HPLC for COX-1 and RIA for COX-2. The balance between COX-1/COX-2 and 5-LOX inhibition can be shifted by modifying the substitution pattern of the phenyl moiety at the 6- and 7-position of the pyrrolizine nucleus. Structure-activity relationships are discussed.

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