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887148-69-8

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887148-69-8 Usage

Description

Benzamide, N-[(1S)-1-cyano-2-[5-cyano-2-(trifluoromethyl)phenoxy]-1-methylethyl]-4-[(trifluoromethyl)thio]is a complex organic compound with a unique molecular structure. It is characterized by the presence of a benzene ring, amide, and cyano groups, as well as a trifluoromethylphenoxy and a trifluoromethylthio group. Benzamide, N-[(1S)-1-cyano-2-[5-cyano-2-(trifluoromethyl)phenoxy]-1-methylethyl]-4-[(trifluoromethyl)thio]exhibits a range of chemical and biological properties, making it a promising candidate for various applications.

Uses

Used in Pharmaceutical Industry:
Benzamide, N-[(1S)-1-cyano-2-[5-cyano-2-(trifluoromethyl)phenoxy]-1-methylethyl]-4-[(trifluoromethyl)thio]is used as a pharmaceutical agent for the treatment of parasitic nematodes. It acts as an anthelmitic, effectively stunning or killing the parasites without causing harm to the host organism. This makes it a valuable tool in combating parasitic infections and improving overall health.
Used in Chemical Research:
Due to its unique molecular structure and properties, Benzamide, N-[(1S)-1-cyano-2-[5-cyano-2-(trifluoromethyl)phenoxy]-1-methylethyl]-4-[(trifluoromethyl)thio]is also used in chemical research for the development of new compounds and materials. Its versatility and reactivity make it a valuable building block for the synthesis of various organic and inorganic compounds, contributing to advancements in fields such as materials science, nanotechnology, and renewable energy.
Used in Pest Control:
Benzamide, N-[(1S)-1-cyano-2-[5-cyano-2-(trifluoromethyl)phenoxy]-1-methylethyl]-4-[(trifluoromethyl)thio]can also be employed in the development of novel pest control agents. Its ability to target and eliminate parasitic nematodes suggests that it may have potential applications in controlling other types of pests, such as insects and mites, in agricultural and horticultural settings. This could lead to the development of more effective and environmentally friendly pest management strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 887148-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,1,4 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 887148-69:
(8*8)+(7*8)+(6*7)+(5*1)+(4*4)+(3*8)+(2*6)+(1*9)=228
228 % 10 = 8
So 887148-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H13F6N3O2S/c1-18(10-28,11-31-16-8-12(9-27)2-7-15(16)19(21,22)23)29-17(30)13-3-5-14(6-4-13)32-20(24,25)26/h2-8H,11H2,1H3,(H,29,30)/t18-/m0/s1

887148-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Monepantel

1.2 Other means of identification

Product number -
Other names N-[(2R)-2-cyano-1-[5-cyano-2-(trifluoromethyl)phenoxy]propan-2-yl]-4-(trifluoromethylsulfanyl)benzamide

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:887148-69-8 SDS

887148-69-8Downstream Products

887148-69-8Relevant articles and documents

Endoparasiticidal compositions

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, (2011/05/05)

The invention relates to a composition for controlling endoparasites in and on animals, which comprises a combination of (A) a compound of formula (I) and (B) paraherquamide A or a derivative or analogue thereof, wherein X and Y are as defined in the claims. The compositions are useful in the control of endoparasites, in particular helminths, in and on warm-blooded animals.

PROCESS FOR THE PREPARATION OF ENANTIOMERS OF AMIDOACETONITRILE COMPOUNDS FROM THEIR RACEMATES

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Page/Page column 8, (2008/06/13)

The invention is directed at a new process for the preparation of pure enantiomers from the racemate of amidoacetonitrile compounds of formula (I) wherein R1, R2 and R3, independently of each other, signify hydrogen, halog

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