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Benzamide, 2,6-difluoro-N-[[[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]is a complex organic chemical compound characterized by the presence of a benzene ring with an amide functional group. It features two fluorine atoms at the 2 and 6 positions on the benzene ring and a carbonyl group connected to an amino group, which is attached to a phenyl ring substituted with a trifluoromethylthio group. This unique molecular structure endows it with potential applications across various fields, such as pharmaceuticals, agrochemicals, and materials science. Further research is necessary to explore its full potential and effects.

64627-98-1

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64627-98-1 Usage

Uses

Used in Pharmaceutical Industry:
Benzamide, 2,6-difluoro-N-[[[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]is used as a pharmaceutical intermediate for the synthesis of various drug candidates. Its unique structure allows it to interact with specific biological targets, making it a promising candidate for the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, Benzamide, 2,6-difluoro-N-[[[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]is used as a precursor for the synthesis of novel agrochemicals with potential applications in pest control and crop protection. Its unique chemical properties enable it to be tailored for specific uses in this field.
Used in Materials Science:
Benzamide, 2,6-difluoro-N-[[[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]is utilized in materials science for the development of new materials with specific properties. Its unique molecular structure allows it to be incorporated into various materials, potentially enhancing their performance in areas such as electronics, coatings, and adhesives.
Further research and studies are required to fully understand the potential uses and effects of Benzamide, 2,6-difluoro-N-[[[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]in these industries and to explore additional applications where its unique properties can be leveraged.

Check Digit Verification of cas no

The CAS Registry Mumber 64627-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64627-98:
(7*6)+(6*4)+(5*6)+(4*2)+(3*7)+(2*9)+(1*8)=151
151 % 10 = 1
So 64627-98-1 is a valid CAS Registry Number.

64627-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-trifluoromethylthiophenyl)-N'-(2,6-difluorobenzoyl)-urea

1.2 Other means of identification

Product number -
Other names 1-(2,6-difluorobenzoyl)-3-(4-trifluoromethylthiophenyl)urea

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:64627-98-1 SDS

64627-98-1Downstream Products

64627-98-1Relevant academic research and scientific papers

CYCLIC COMPOUND, PROCESS FOR PRODUCING THE SAME, AND PEST CONTROL AGENT

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Page 137, (2010/02/09)

A compound represented by the formula: wherein, A represents a group represented by the formula: CY1Y2OCY3Y4, CY1Y2SOnCY3Y4, CY1Y2NRCY3Y4, CY1=NCY3Y4 or CY1Y2N=CY3 (wherein n is 0, 1, or 2, and Y1, Y2, Y3, and Y4 each independently represents hydrogen, alkyl, or haloalkyl); R represents hydrogen, halogen, an optionally substituted hydrocarbon group, etc.; Q1 represents substituted phenyl or a substituted aromatic heterocyclic group; and Q2 represents substituted phenyl, alkyl, or haloalkyl, or a salt. thereof; a process for producing the. compound or a salt thereof; and an insecticide containing. the same. Besides being applicable by spraying, the insecticide can be used for soil treatment and seed treatment.

Use of acyl urea compounds for controlling endoparasites and ectoparasites of warm-blooded animals

-

, (2008/06/13)

A method of systemically controlling endoparasites and ectoparasites of warm-blooded animals by orally or percutaneously administering to the animal a parasiticidally effective amount of an acyl urea compound.

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