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4,6-Bis-(trichloromethyl)-2-styryl-1,3,5-triazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42880-03-5

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42880-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42880-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,8 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42880-03:
(7*4)+(6*2)+(5*8)+(4*8)+(3*0)+(2*0)+(1*3)=115
115 % 10 = 5
So 42880-03-5 is a valid CAS Registry Number.

42880-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-phenylethenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names -

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:42880-03-5 SDS

42880-03-5Upstream product

42880-03-5Downstream Products

42880-03-5Relevant academic research and scientific papers

Process for preparing chromophore-substituted vinyl-halomethyl-s-triazines

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, (2008/06/13)

An improved method for the preparation of chromophore-substituted vinyl-halomethyl-s-triazines especially 2-(p-methoxystyryl)-4,6-bis-(trichloromethyl)-s-triazine. In the known preparation of these compounds, a two step procedure is utilized wherein an intermediate reaction product has to be isolated. This step of separating the intermediate is eliminated in the present process by dissolving the crude reaction product obtained in the first step in toluene, removing excess hydrogen chloride gas and catalysts by purging the reaction product solution with an inert gas, and then reacting p-anisaldehyde with the toluene solution of the reaction product mixture using piperidinium acetate catalyst to obtain 2-(p-methoxystyryl)-4,6-bis-(trichloromethyl)-s-triazine. As a further improvement of the art the Knoevenagel-type condensation is run until no further water is evolved. At this point the product formed is isolated by filtration and a like amount of catalyst as a second charge is added. Again, the reaction is carried out until no further water is evolved and further product is isolated by filtration.

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