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

60253-50-1

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60253-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60253-50-1 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, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60253-50:
(7*6)+(6*0)+(5*2)+(4*5)+(3*3)+(2*5)+(1*0)=91
91 % 10 = 1
So 60253-50-1 is a valid CAS Registry Number.

60253-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 1,3,5-tris(4-fluorophenyl)-1,3,5-triazinane-2,4,6-trion

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:60253-50-1 SDS

60253-50-1Downstream Products

60253-50-1Relevant academic research and scientific papers

Aluminium-catalysed isocyanate trimerization, enhanced by exploiting a dynamic coordination sphere

Bahili, Mohammed A.,Stokes, Emily C.,Amesbury, Robert C.,Ould, Darren M. C.,Christo, Bashar,Horne, Rhian J.,Kariuki, Benson M.,Stewart, Jack A.,Taylor, Rebekah L.,Williams, P. Andrew,Jones, Matthew D.,Harris, Kenneth D. M.,Ward, Benjamin D.

supporting information, p. 7679 - 7682 (2019/07/08)

Main-group metals are inherently labile, hindering their use in catalysis. We exploit this lability in the synthesis of isocyanurates. For the first time we report a highly active catalyst that trimerizes alkyl, allyl and aryl isocyanates, and di-isocyanates, with low catalyst loadings under mild conditions, using a hemi-labile aluminium-pyridyl-bis(iminophenolate) complex.

Potassium complexes containing bidentate pyrrole ligands: Synthesis, structures, and catalytic activity for the cyclotrimerization of isocyanates

Guo, Zhiqiang,Xu, Yuan,Wu, Xiaoqin,Wei, Xuehong,Xi, Chanjuan

supporting information, p. 8116 - 8121 (2019/06/19)

Bidentate pyrrolyl ligands, 2-(t-butyliminomethyl)pyrrole and 2-(t-butylaminomethyl)pyrrole, reacted with KH to give complexes [C4H3N(2-CHNtBu)K(THF)]n (1) and [C4H3N(2-CH2NHsup

Isocyanurate Formation During Oxazolidinone Synthesis from Epoxides and Isocyanates Catalysed by a Chromium(Salphen) Complex

Wu, Xiao,Mason, Jess,North, Michael

, p. 12937 - 12943 (2017/09/25)

Chromium(salphen) complex 10 is found to be a catalyst for the preparation of oxazolidinones from epoxides and isocyanates. Using the optimal reaction conditions (1.5 mol % of chromium(salphen) complex 10 at 80 °C in toluene for 4 hours), six epoxides wer

Generation of low-valent alkoxy niobium from Nb(OEt)5 and Grignard reagents and their use as catalysts in the cyclotrimerization of isocyanates

Ozaki, Makoto,Obora, Yasushi,Tada, Yusuke,Ishii, Yasutaka

, p. 109 - 113 (2013/10/01)

A new highly active low-valent alkoxyniobium species has been developed following the reaction of Nb(OEt)5 with Grignard reagent such as i-PrMgCl or EtMgCl, with the material behaving as an efficient catalyst for cyclotrimerization reaction of isocyanates. In this reagent system, the existence of a lowvalent niobium species was confirmed by the formation of the niobiumealkyne complex prepared from the Nb(OEt)5/Grignard reagent system and an alkyne. Furthermore, the hydrolysis and diallylation reactions of the niobiumealkyne complex provided further confirmation of its existence, with corresponding (Z)-alkene and diallylated products being isolated in good yields.

Polymer-supported, carbon dioxide-protected n-heterocyclic carbenes: Synthesis and application in organo- and organometallic catalysis

Pawar, Gajanan Manohar,Buchmeiser, Michael R.

scheme or table, p. 917 - 928 (2010/06/15)

The synthesis of a resin-supported, carbon dioxide-protected N-heterocyclic carbene (NHC) and its use in organocatalysis and organometallic catalysis are described. The resin-bound carbon dioxide-protected NHC-based catalyst was prepared via ring-opening

CO2 and SnII adducts of N-heterocyclic carbenes as delayed-action catalysts for polyurethane synthesis

Bantu, Bhasker,Pawar, Gajanan Manohar,Decker, Ulrich,Wurst, Klaus,Schmidt, Axel M.,Buchmeiser, Michael R.

experimental part, p. 3103 - 3109 (2009/11/30)

A series of CO2-protected pyrimidin-2-ylidenes as well as 1,3-dimesitylimidazol-2-ylidene and dimesitylimidazolin-2-ylidene complexes of SnII have been prepared. Selected single-crystal X-ray structures are reported. The new compound

The aza Curtius rearrangement

Yagupolskii, Lev M.,Shelyazhenko, Svetlana V.,Maletina, Irina I.,Petrik, Vitalij N.,Rusanov, Eduard B.,Chernega, Alexander N.

, p. 1225 - 1233 (2007/10/03)

On interaction of N-(trifluoromethylsulfonyl)carboximidoyl chlorides (analogs of acyl chlorides in which the carbonyl oxygen atom is substituted by the more strongly electron-withdrawing =NSO2CF3 group) with sodium azide in glyme or acetonitrile at -5 to +10 °C, dinitrogen is eliminated quantitatively and carbodiimides RN=C=NSO2CF3 are formed in high yield. In other words, an aza Curtius rearrangement occurs. The carbodiimides react with water, alcohols, and secondary amines to give corresponding ureas, isoureas, and guanidine derivatives. Imidoyl chlorides with substituents other than SO2RF do not enter into the aza Curtius reaction.

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