Welcome to LookChem.com Sign In|Join Free
  • or
5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]4(ethylsulfinyl)-1H-pyrazole-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

623151-90-6

Post Buying Request

623151-90-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

623151-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623151-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,5 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 623151-90:
(8*6)+(7*2)+(6*3)+(5*1)+(4*5)+(3*1)+(2*9)+(1*0)=126
126 % 10 = 6
So 623151-90-6 is a valid CAS Registry Number.

623151-90-6Upstream product

623151-90-6Downstream Products

623151-90-6Relevant academic research and scientific papers

Phenylpyrazole Insecticide Photochemistry, Metabolism, and GABAergic Action: Ethiprole Compared with Fipronil

Caboni, Pierluigi,Sammelson, Robert E.,Casida, John E.

, p. 7055 - 7061 (2003)

Ethiprole differs from fipronil, the major phenylpyrazole insecticide, only in an ethylsulfinyl substituent replacing the trifluoromethylsulfinyl moiety. This study compares their photochemistry, metabolism, action at the γ-aminobutyric acid (GABA) receptor, and insecticidal potency. On exposure to sunlight as a thin film, ethiprole undergoes oxidation (major), reduction, and desethylsulfinylation but not desulfinylation whereas the major photoreaction for fipronil is desulfinylation. Metabolic sulfone formation is more rapid with ethiprole than fipronil in human expressed CYP3A4 in vitro and mouse brain and liver in vivo. High biological activity is observed for the sulfide, sulfoxide, sulfone, and desulfinyl derivatives in both the ethiprole and the fipronil series in GABA receptor assays (human recombinant β3 homomer and house fly head membranes) with [3H]EBOB and in topical toxicity to house flies with and without the P450-inhibiting synergist piperonyl butoxide. On an overall basis, the ethiprole series is very similar in potency to the fipronil series.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 623151-90-6