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N-(2,4,6-Trichlorophenyl)maleimide is a white to beige crystalline compound with a chemical structure that features a trichlorophenyl group attached to a maleimide moiety. This unique structure endows it with specific chemical properties that make it suitable for various applications, particularly in the field of polymer chemistry.

13167-25-4

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13167-25-4 Usage

Uses

Used in Marine Antifouling Field:
N-(2,4,6-Trichlorophenyl)maleimide is used as a key component in the preparation of self-polishing branched polymer antifouling resin. This application is crucial for the marine industry, as it helps in preventing the growth of marine organisms on the hulls of ships and other submerged structures. The self-polishing property of the resin allows it to maintain its effectiveness over time, reducing the need for manual cleaning and the associated costs and environmental impacts.
The incorporation of N-(2,4,6-Trichlorophenyl)maleimide into the antifouling resin is attributed to its chemical properties, which contribute to the resin's self-polishing behavior and resistance to marine fouling. This makes it an essential ingredient in the development of advanced marine coatings that protect ships and other marine structures from the detrimental effects of biofouling.

Check Digit Verification of cas no

The CAS Registry Mumber 13167-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,6 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13167-25:
(7*1)+(6*3)+(5*1)+(4*6)+(3*7)+(2*2)+(1*5)=84
84 % 10 = 4
So 13167-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H4Cl3NO2/c11-5-3-6(12)10(7(13)4-5)14-8(15)1-2-9(14)16/h1-4H

13167-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4,6-Trichlorophenyl)-1H-pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-(2,4,6-trichlorophenyl)pyrrole-2,5-dione

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:13167-25-4 SDS

13167-25-4Downstream Products

13167-25-4Relevant academic research and scientific papers

Synthesis method for increasing yield of N-(2,4,6-trichlorophenyl)maleimide

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Paragraph 0021, (2016/11/21)

The invention discloses a synthesis method for increasing the yield of N-(2,4,6-trichlorophenyl)maleimide. The synthesis method comprises the steps that firstly, an N-(2,4,6-trichlorophenyl)maleimide intermediate product is synthesized at the room temperature, and then the intermediate product is catalyzed and dehydrated to obtain N-(2,4,6-trichlorophenyl)maleimide. According to the synthesis method, the reaction temperature is low, the industrial cost is low, little harm is caused, and the yield can reach 95%.

Use of riboflavin and flavin derivatives as chitinase inhibitors

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, (2008/06/13)

The invention relates to the use of riboflavin and of flavin derivatives with chitinase-inhibitory action for controlling arthropods, nematodes and chitin-containing fungi.

Synthesis of N-halogenated phenyl maleimide compounds with tin containing catalysts

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, (2008/06/13)

A process for the preparation of N-brominated or N-chlorinated phenylmaleimide by reacting maleic anhydride and a brominated or chlorinated aniline compound at temperatures of from about 100° C. to about 210° C. in the presence of tin containing catalyst compound and optionally an inert solvent.

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