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2-Chloro-4-(pentafluorothio)aniline, 97% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

165114-85-2

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165114-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 165114-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,1,1 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 165114-85:
(8*1)+(7*6)+(6*5)+(5*1)+(4*1)+(3*4)+(2*8)+(1*5)=122
122 % 10 = 2
So 165114-85-2 is a valid CAS Registry Number.

165114-85-2Relevant academic research and scientific papers

1,2,3-TRIAZOLE DERIVATIVE AND INSECTICIDE AND ACARICIDE CONTAINING SAID DERIVATIVE AS ACTIVE INGREDIENT

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Paragraph 0246; 0247, (2018/10/30)

The present invention provides a 1,2,3-triazole derivative and an insecticide or acaricide containing the 1,2,3-triazole derivative as an active ingredient.

PENTAFLUOROSULPHOLANE-CONTAINING ANTIDIABETIC COMPOUNDS

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Page/Page column 50, (2010/08/08)

This invention provides for certain pentafluorosulpholane-containing compounds of the formula or a pharmaceutically acceptable salt, ester, solvate or prodrug thereof, wherein the variables are defined herein; the inventive compounds are agonists of the G

N-(1-ARYLPYRAZOL-4L)SULFONAMIDES AND THEIR USE AS PARASITICIDES

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Page/Page column 138-139, (2010/02/14)

The invention relates to a sulfonamide compound of formula (I) or a pharmaceutically, veterinarily or agriculturally acceptable salt or solvate thereof, where the groups R1-R5 are described in the description, to compositions comprising such compounds, processes for their synthesis and their use as parasiticides.

Synthesis of some arylsulfur pentafluoride pesticides and their relative activities compared to the trifluoromethyl analogues

Crowley, Patrick J.,Mitchell, Glynn,Salmon, Roger,Worthington, Paul A.

, p. 138 - 142 (2007/10/03)

Examples of pesticides containing an arylsulfur pentafluoride group were made and their biological activities compared to the corresponding trifluoromethyl analogues. A phenylsulfur pentafluoride analogue of the insecticide fipronil, screened against a resistant strain of Musca domestica, showed higher activity than the corresponding trifluoromethyl analogue.

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