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[1-(4-Butoxy-phenyl)-meth-(E)-ylidene]-phenyl-amine is a complex organic compound characterized by its unique molecular structure. It features a phenylamine core, with one of its phenyl rings substituted at the para position with a butoxy group. The butoxy group is an alkyl chain with four carbon atoms attached to an oxygen atom, which is in turn connected to the phenyl ring. The other phenyl ring is connected to the first through a methine bridge (a carbon atom double-bonded to two other carbon atoms), with the double bond being in the E configuration, indicating the trans arrangement of the substituents around the double bond. [1-(4-Butoxy-phenyl)-meth-(E)-ylidene]-phenyl-amine is likely to be involved in various chemical reactions and may have applications in the synthesis of pharmaceuticals, dyes, or other specialty chemicals due to its specific structural features.

5219-44-3

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5219-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5219-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5219-44:
(6*5)+(5*2)+(4*1)+(3*9)+(2*4)+(1*4)=83
83 % 10 = 3
So 5219-44-3 is a valid CAS Registry Number.

5219-44-3Relevant academic research and scientific papers

Quinoline-4-methyl esters as human nonpancreatic secretory phospholipase A2 inhibitors

Wu, Yiran,Chen, Zheng,Liu, Ying,Yu, Lanlan,Zhou, Lu,Yang, Suijia,Lai, Luhua

, p. 3361 - 3366 (2011/07/29)

A series of novel fused heterocycle methyl esters were designed and synthesized as human nonpancreatic secretory phospholipase A2 (hnps-PLA2) competitive inhibitors. Among the 22 synthesized compounds, 17 quinoline-4-methyl esters displayed hnps-PLA2 inhibition activity in the in vitro bioassay. The IC50 value for the best compound 3o was 1.5 μM. The structure-inhibition-activity relationships of the compounds were studied using molecular docking.

Synthesis and photophysical properties of 2-Styrylquinazolin-4-ones

Trashakhova,Nosova,Valova,Slepukhin,Lipunova,Charushin

body text, p. 753 - 761 (2011/08/22)

Trans-2-Styryl-substituted 3H-, 3-phenyl-, and 3-naphthylquinazolin-4-ones and their 6,7-difl uoro derivatives were synthesized by condensation of appropriate 2-methylquinazolin-4-ones with aromatic aldehydes or by the transformation of the heterocycle of 2-methyl-3,1-benzoxazin-4-one under the action of benzylidenephenylamines. Pleiades Publishing, Ltd., 2011.

Synthesis and antimicrobial activity of 1-(p-substituted)phenyl-3-(p-alkoxy)phenyl-4-phenyl-azetidin-2-ones

Vittoria Diurno,Cristinziano,Mazzoni,Piscopo,Bolognese

, p. 143 - 148 (2007/10/02)

A series of 1-(p-substituted)phenyl)-3-(p-alkoxy)phenyl-4-phenyl-azetidin-2-ones 1a-20a, was synthesized and characterized. Their antimicrobial activity, against Gram+ and Gram - bacteria and Fungi, was tested. The compounds 8a, 13a, 14a, 18a and 6a, 9a,

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