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5(4H)-Oxazolone, 2-(3-methoxy-2-methylphenyl)-4-methyl-4-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

551964-00-2

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  • 5(4H)-Oxazolone,2-(3-methoxy-2-methylphenyl)-4-methyl-4-(1-methylethyl)-

    Cas No: 551964-00-2

  • USD $ 1.9-2.9 / Gram

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551964-00-2 Usage

Heterocyclic compound

5(4H)-Oxazolone has a five-membered ring containing both oxygen and nitrogen atoms.

Organic compound

2-(3-methoxy-2-methylphenyl)-4-methyl-4-(1-methylethyl)is composed of carbon, hydrogen, and oxygen atoms with various substituents.

Substituents

The organic compound has a methoxy group, a methyl group, and an isopropyl group attached to its phenyl ring.

Derivative of methylphenylpiperazine

The compound is derived from a methylphenylpiperazine structure, which is a type of chemical structure commonly found in pharmaceuticals.

Pharmacological properties

The compound exhibits potential pharmacological properties, such as acting as a serotonin-releasing agent.

Potential applications

The combination of 5(4H)-Oxazolone and 2-(3-methoxy-2-methylphenyl)-4-methyl-4-(1-methylethyl)may contribute to the development of new drugs or therapeutic agents in the field of pharmacology or medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 551964-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,1,9,6 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 551964-00:
(8*5)+(7*5)+(6*1)+(5*9)+(4*6)+(3*4)+(2*0)+(1*0)=162
162 % 10 = 2
So 551964-00-2 is a valid CAS Registry Number.

551964-00-2Relevant articles and documents

Ketone ligands for modulating the expression of exogenous genes via an ecdysone receptor complex

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Page 33, (2008/06/13)

This invention relates to a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding domain; a transactivation domain; and a ligand is contacted with a DNA construct comprising:

Synthesis and SAR of α-acylaminoketone ligands for control of gene expression

Tice, Colin M.,Hormann, Robert E.,Thompson, Christine S.,Friz, Jennifer L.,Cavanaugh, Caitlin K.,Michelotti, Enrique L.,Garcia, Javier,Nicolas, Ernesto,Albericio, Fernando

, p. 475 - 478 (2007/10/03)

A lead discovery library and a follow-up focused library of α-acylaminoketones were designed based on known dibenzoylhydrazine ecdysone agonists, including GS-E. The compounds were assayed in mammalian cells expressing the ecdysone receptor from Bombyx mori for their ability to cause expression of a reporter gene downstream of an ecdysone response element. The most potent α-acylaminoketones were comparable to GS-E in this assay.

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