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1-(2,2-Dimethoxyethyl)-1,6-dihydro-6-oxo-2-phenyl-5-pyrimidinecarboxylic acid, commonly known as Deltamethrin, is a synthetic pyrethroid insecticide belonging to the Type II pyrethroids. It is characterized by its potent action on the nervous system of insects, leading to paralysis and death. Deltamethrin is recognized for its high effectiveness and rapid action, with relatively low toxicity to humans and other mammals, making it a preferred choice in various applications.

293329-57-4

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293329-57-4 Usage

Uses

Used in Agricultural Applications:
Deltamethrin is used as an insecticide for controlling a broad spectrum of pests, such as insects and mites, in agricultural settings. Its fast-acting and potent nature makes it a valuable tool in protecting crops and ensuring a stable food supply.
Used in Public Health Applications:
In public health, Deltamethrin is utilized to control pests that can transmit diseases or cause discomfort to humans. Its effectiveness in targeting a wide range of insects and mites makes it a crucial component in maintaining a healthy living environment.

Check Digit Verification of cas no

The CAS Registry Mumber 293329-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,2 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 293329-57:
(8*2)+(7*9)+(6*3)+(5*3)+(4*2)+(3*9)+(2*5)+(1*7)=164
164 % 10 = 4
So 293329-57-4 is a valid CAS Registry Number.

293329-57-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,2-dimethoxyethyl)-6-oxo-2-phenylpyrimidine-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:293329-57-4 SDS

293329-57-4Relevant academic research and scientific papers

Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade

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Page/Page column 108-109, (2010/01/31)

The invention relates to substituted polycyclic aryl and heteroaryl pyrimidinone compounds useful as inhibitors of serine proteases of the coagulation cascade and compounds, compositions and methods for anticoagulant therapy for the treatment and prevention of a variety of thrombotic conditions including coronary artery and cerebrovascular diseases.

Nonpeptidic inhibitors of human leukocyte elastase. 5. Design, synthesis, and X-ray crystallography of a series of orally active 5-aminopyrimidin-6- one-containing trifluoromethyl ketones

Veale,Bernstein,Bryant,Ceccarelli,Damewood Jr.,Earley,Feeney,Gomes,Kosmider,Steelman,Thomas,Vacek,Williams,Wolanin,Woolson

, p. 98 - 108 (2007/10/02)

The effects of changes in substitution in a series of 5-amino-2- pyrimidin-6-ones on both in vitro activity and oral activity in an acute hemorrhage assay have been explored. These compounds contained either a trifluoromethyl ketone or a boronic acid moiety to bind covalently to the Ser-195 hydroxyl of human leukocyte elastase (HLE). Boronic acid-containing inhibitors were found to be more potent than the corresponding trifluoromethyl ketones in vitro but were less active upon oral administration. Compound 13b was found to offer the best combination of oral potency, duration of action, and enzyme selectivity and, as such, was selected for further biological testing. X-ray crystallography of a cocrystallized complex of compound 19m and porcine pancreatic elastase demonstrated that the inhibitor is bound to the enzyme in a manner similar to that found previously for a closely related series of pyridone-containing inhibitors of HLE.

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