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5-isopropyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione is a complex organic compound with the molecular formula C15H18N2O3. It is a derivative of pyrimidinedione, featuring an isopropyl group at the 5-position and a 3,5-dimethylphenoxy group at the 6-position. This chemical is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a herbicide. Its structure provides it with specific biological activity, making it a subject of interest in the development of new chemical entities for controlling weed growth in agricultural settings. The compound's unique arrangement of functional groups contributes to its effectiveness and selectivity in targeting specific plant species.

171048-76-3

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171048-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171048-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,4 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 171048-76:
(8*1)+(7*7)+(6*1)+(5*0)+(4*4)+(3*8)+(2*7)+(1*6)=123
123 % 10 = 3
So 171048-76-3 is a valid CAS Registry Number.

171048-76-3Upstream product

171048-76-3Relevant academic research and scientific papers

NOVEL HIV REVERSE TRANSCRIPTASE INHIBITORS

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Page/Page column 430, (2009/03/07)

The invention is related to compounds of Formula (I) or a pharmaceutically acceptable salt, solvate, ester, and/ or phosphonate thereof, compositions containing such compounds, and therapeutic methods that include the administration of such compounds.

Antiviral 2,4-pyrimidinedione derivatives and process for the preparation thereof

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Page/Page column 20; 27; 28, (2010/02/06)

2,4-pyrimidinedione derivatives of formula (I) having high antiviral activity against wild-type and mutant HIV-1 and low toxicity are useful for treating AIDS (I) wherein: R1is a C6-10aryl or C3-10heteroaryl group optional

Antiviral 2, 4-pyrimidinedione derivatives

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, (2008/06/13)

Novel 2,4-pyrimidinedione compounds, and pharmaceutically acceptable salts thereof which possess good antiviral activities, and specifically represented by the following formula(I): STR1 wherein: R 1 represents an unsubstituted or substituted allyl group represented by CH 2 CH CR 5 R 6 or an unsubstituted or substituted propargyl group represented by CH 2 C CR 7 wherein R 5, R 6 and R 7 are each independently a hydrogen atom; a methyl group optionally substituted with a halogen atom, or a C 1-10 carbonyloxy, hydroxy, azido, cyano, optionally substituted amino, optionally substituted phosphonyl, optionally substituted phenyl, C 3-10 heteroaryl, C 1-3 alkoxy or benzyloxy radical; a C 2-10 alkyl or alkenyl group; a cyclopropyl group; an optionally substituted phenyl group; a C 3-10 heteroaryl group; a C 1-10 ester group; or an optionally substituted C 1-10 alkylamide group;R 2 represents a halogen atom, an optionally substituted C 1-5 alkyl, C 3-6 cycloalkyl, C 2-8 alkenyl, C 2-8 alkynyl group or a benzyl group;R 3 and R 4 represent independently a hydrogen or halogen atom, or a hydroxy, C 1-3 alkyl, fluoromethyl, C 1-3 alkoxy, amino, C 2-6 alkylester or C 2-7 alkylamide group;A represents an oxygen or sulfur atom;Z represents an oxygen or sulfur atom; a carbonyl group; an amino group; or a methylene group optionally substituted with at least one selected from the group consisting of a halogen atom, and a cyano, hydroxy, azido, amino, C 1-3 alkylamide, C 1-4 ester, and nitro groups.

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