27277-66-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the specific arrangement of atoms and bonds in the compound.
Explanation
The compound is used in agriculture to control pests and weeds.
Explanation
By disrupting the process of photosynthesis, the compound causes the death of the target organisms.
Explanation
The compound is effective against various types of pests and weeds, making it a versatile tool in agriculture.
Explanation
The compound can be harmful to unintended organisms, so care should be taken to minimize exposure to non-target species.
Chemical structure
1,2,4-Triazine-3,5(2H,4H)-dione, 2-[(2,4-dichlorophenyl)methyl]-
Application
Insecticide and herbicide
Mode of action
Inhibits photosynthesis in target organisms
Effectiveness
Wide range of pests and weeds
Caution
Toxic to non-target organisms
Check Digit Verification of cas no
The CAS Registry Mumber 27277-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,7 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27277-66:
(7*2)+(6*7)+(5*2)+(4*7)+(3*7)+(2*6)+(1*6)=133
133 % 10 = 3
So 27277-66-3 is a valid CAS Registry Number.
27277-66-3Relevant academic research and scientific papers
Anticoccidial derivatives of 6 azauracil. I. Enhancement of activity by benzylation of nitrogen 1. Observations on the design of nucleotide analogues in chemotherapy
Mylari,Miller,Howes Jr.,Figdor,Lynch,Koch
, p. 475 - 483 (2007/10/09)
Benzylation of 6-azauracil at N-1 (which corresponds to the point of attachment of the ribose phosphate unit in pyrimidine nucleotides) has been found to augment its anticoccidial activity fourfold. The high potency of 1-benzyl-6-azauracil is ascribed to a combination of intrinsic activity, efficient oral absorption, and a moderate rate of excretion. Metabolism experiments using 1-benzyl-6-azauracil labeled with 14C in the heterocycle and (separately) in the side chain showed that, in the drug accounted for, no cleavage had occurred. Additional activity increases were achieved by introducing small, electron-withdrawing substituents in the meta and/or para position(s) of the benzyl group. One of the most active derivatives, 1-(3-cyanobenzyl)-6-azauracil, is about 16 times as potent as 6-azauracil.
