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1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris(3-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60253-49-8

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60253-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60253-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,5 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60253-49:
(7*6)+(6*0)+(5*2)+(4*5)+(3*3)+(2*4)+(1*9)=98
98 % 10 = 8
So 60253-49-8 is a valid CAS Registry Number.

60253-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-tris(3-fluorophenyl)-1,3,5-triazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(3-fluorophenyl)

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:60253-49-8 SDS

60253-49-8Downstream Products

60253-49-8Relevant academic research and scientific papers

Highly efficient cyclotrimerization of isocyanates using N-heterocyclic olefins under bulk conditions

Li, Chengkai,Zhao, Wuchao,He, Jianghua,Zhang, Yuetao

, p. 12563 - 12566 (2019)

With a catalyst loading as low as 0.005%, high to excellent yields of isocyanurates could be achieved from N-heterocyclic olefin mediated organocatalytic cyclotrimerization of a wide range of isocyanates under bulk conditions. Experimental details coupled with structural characterization of the key intermediates led to comprehensive mechanistic studies of cyclotrimerization.

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