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1,3-dibromo-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

864736-96-9

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864736-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 864736-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,7,3 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 864736-96:
(8*8)+(7*6)+(6*4)+(5*7)+(4*3)+(3*6)+(2*9)+(1*6)=219
219 % 10 = 9
So 864736-96-9 is a valid CAS Registry Number.

864736-96-9Relevant academic research and scientific papers

THIAZOLES AS MODULATORS OF RORyt

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Page/Page column 98, (2016/05/19)

The present invention comprises compounds of Formula I. Formula I wherein: R1, R2, R3, R4, R5, R7, R8, and (A) are defined in the specification. The invention also comprises a co

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.

BORON-CONTAINING SMALL MOLECULES

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Paragraph 0212, (2013/06/04)

This invention provides novel compounds, methods of using the compounds, and pharmaceutical formulations comprising the compounds.

Process for Production of 2-(Substituted Phenyl)-3,3,3-Trifluoropropene Compound

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Page/Page column 6, (2010/07/04)

There is provided a novel process for production of a 2-(substituted phenyl)-3,3,3-trifluoropropene. Disclosed is a process for production of a 2-(substituted phenyl)-3,3,3-trifluoropropene compound represented by the formula (7) or a salt thereof The process comprises reacting a compound represented by the formula (1) (X is an alkyl group, etc.) with a compound represented by the formula (2) (Y is a halogen atom, etc.) in the presence of a catalyst represented by the formula (3) (M is an ion of a metal belonging to Group 10 on the elementary periodic table which has an oxidation state number of 1 to 8; G is a unidentate or multidentate ligand; L is a phosphine compound represented by the formula (4) which is bound to the center metal M or is a carbene selected from those represented by the formulae (5) and (6), provided that L's may be same as or different from one another when a is 2 to 5; A represents a univalently or multivalently charged anion; b represents an integer of 1 to 3; a represents an integer of 1 to 5·b; c represents 0 or an integer of 1 to 4·b; and n represents an integer of 1 to 6).

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