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928783-84-0

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928783-84-0 Usage

Functional groups

Chlorine atoms (3), Fluorine atom (1), Benzene ring, 3,3,3-trifluoroprop-1-en-2-yl group

Structural features

a. Chlorine atoms are attached to the 1st and 3rd carbon atoms of the benzene ring
b. Fluorine atom is attached to the 2nd carbon atom of the benzene ring
c. 3,3,3-trifluoroprop-1-en-2-yl group is attached to the 5th carbon atom of the benzene ring

Physical properties

a. Likely to be a solid at room temperature due to the presence of multiple halogen atoms
b. May have a high melting point due to strong intermolecular forces
c. Low solubility in water due to the presence of nonpolar groups
d. High solubility in organic solvents like dichloromethane or acetone

Chemical properties

a. Reactive towards nucleophiles due to the presence of electron-withdrawing groups
b. Susceptible to electrophilic aromatic substitution reactions at the unsubstituted carbon atoms of the benzene ring
c. May undergo halogenation reactions with other halogens
d. Potential for hydrogen bonding with polar solvents due to the presence of fluorine atoms

Potential applications

a. Building block in organic synthesis
b. Development of pharmaceuticals
c. Development of agrochemicals
d. Development of materials science

Safety considerations

a. Handle with care due to potential reactivity
b. Thorough investigation of properties before industrial or commercial applications
c. Use appropriate protective equipment and follow safety protocols during handling and storage

Check Digit Verification of cas no

The CAS Registry Mumber 928783-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,7,8 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 928783-84:
(8*9)+(7*2)+(6*8)+(5*7)+(4*8)+(3*3)+(2*8)+(1*4)=230
230 % 10 = 0
So 928783-84-0 is a valid CAS Registry Number.

928783-84-0Downstream Products

928783-84-0Relevant articles and documents

Substituted benzamide isoxazoline derivative or pesticide acceptable salt, composition and application of substituted benzamide isoxazoline derivative or pesticide acceptable salt

-

, (2021/11/03)

The invention belongs to the field of pesticides, and particularly relates to a substituted benzamide isoxazoline derivative or a pesticide acceptable salt, a composition and application thereof, the compound has a structure as shown in a formula (I), and the definition of each group in the formula is shown in the specification. The substituted benzamide isoxazoline derivatives of the present invention have higher insecticidal or acaricidal activity than known compounds.

Isoxazoline substituted benzamide derivative as well as preparation method and application thereof

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Paragraph 0121-0122; 0125-0126, (2020/11/23)

The invention belongs to the technical field of insecticides and acaricides, and particularly relates to an isoxazoline substituted benzamide derivative as well as a preparation method and applicationthereof. The invention particularly provides a compound shown as a formula (I) or salt thereof. The compound shown as the formula (I) has good activity on various pests and mites in agriculture or other fields. Moreover, the compounds can achieve a very good prevention and treatment effect at a very low dosage, so that the compounds can be used for preparing insecticides and/or acaricides, and have a relatively good application prospect.

4-Azolylphenyl isoxazoline insecticides acting at the GABA gated chloride channel

Lahm, George P.,Cordova, Daniel,Barry, James D.,Pahutski, Thomas F.,Smith, Ben K.,Long, Jeffrey K.,Benner, Eric A.,Holyoke, Caleb W.,Joraski, Kathleen,Xu, Ming,Schroeder, Mark E.,Wagerle, Ty,Mahaffey, Michael J.,Smith, Rejane M.,Tong, My-Hahn

, p. 3001 - 3006 (2013/06/26)

Isoxazoline insecticides have been shown to be potent blockers of insect GABA receptors with excellent activity on a broad pest range, including Lepidoptera and Hemiptera. Herein we report on the synthesis, biological activity and mode-of-action for a class of 4-heterocyclic aryl isoxazoline insecticides.

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