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1785-02-0

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1785-02-0 Usage

General Description

Aurora KA-3367 is a chemical compound that is a light yellow liquid at room temperature. It is a blend of surfactants designed for use as a cleaner and degreaser in a wide range of industrial and commercial applications. This chemical is formulated to effectively remove oils, greases, and other contaminants from various surfaces, including metal, concrete, and plastic. It is also designed to be water-soluble and non-flammable, making it a safer option for use in industrial settings. Additionally, Aurora KA-3367 is biodegradable, making it an environmentally friendly option for cleaning and degreasing operations.

Check Digit Verification of cas no

The CAS Registry Mumber 1785-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1785-02:
(6*1)+(5*7)+(4*8)+(3*5)+(2*0)+(1*2)=90
90 % 10 = 0
So 1785-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H15N3O3/c25-19-22(16-10-4-1-5-11-16)20(26)24(18-14-8-3-9-15-18)21(27)23(19)17-12-6-2-7-13-17/h1-15H

1785-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-triphenyl-1,3,5-triazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names Phenyl isocyanurate

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:1785-02-0 SDS

1785-02-0Relevant articles and documents

Lai, Richard,Mabille, Sylvain,Croux, Alain,Bot, Sylvie Le

, p. 463 - 466 (1991)

Phosphorylation of isocyanates and aldehydes mediated by multifunctional n-phosphine oxide-substituted imidazolylidenes

Hoshimoto, Yoichi,Asada, Takahiro,Hazra, Sunit,Ohashi, Masato,Ogoshi, Sensuke

, p. 1211 - 1213 (2017)

The direct syntheses of imidic-phosphinic mixed anhydrides and phosphinates were accomplished via phosphorylation of isocyanates or aldehydes with N-phosphine oxide-substituted imidazolylidenes (PoxIms) that are equipped with both nucle-ophilic carbene an

Development of high-performance networked polymers consisting of isocyanurate structures based on selective cyclotrimerization of isocyanates

Moritsugu, Masaki,Sudo, Atsushi,Endo, Takeshi

, p. 5186 - 5191 (2011)

Selective and quantitative cyclotrimerization of p-tolylisocyanate proceeded by using sodium p-toluenesulfinate as a catalyst and 1,3-dimethylimidazolidinone as a solvent. Exploitation of this system to the cyclotrimerization of methylene diphenyl 4,4′-di

New Insights in Frustrated Lewis Pair Chemistry with Azides

Boom, Devin H. A.,Jupp, Andrew R.,Nieger, Martin,Ehlers, Andreas W.,Slootweg, J. Chris

, p. 13299 - 13308 (2019)

The geminal frustrated Lewis pair (FLP) tBu2PCH2BPh2 (1) reacts with phenyl-, mesityl-, and tert-butyl azide affording, respectively, six, five, and four-membered rings as isolable products. DFT calculations revealed that

Transition-metal-mediated activation of arylisocyanates in supercritical carbon dioxide

Montilla, Francisco,Clara, Elisabete,Avilés, Teresa,Casimiro, Teresa,Aguiar Ricardo, Ana,Nunes Da Ponte, Manuel

, p. 227 - 232 (2001)

The reactivity of arylisocyanates in supercritical carbon dioxide (scCO2) was studied using the easily available complexes CpCo(CO)2, CpCoPPh3Me2 and Ni(cod)2 as catalysts. A study of the solubility o

'Push-Pull' and spirobicyclic structures by reacting N-methyl cyclic ketene-N,X (X=S, O)-acetals with isocyanates and isothiocyanates

Zhou, Aihua,Cao, Liwei,Li, Haiqing,Liu, Zhuqing,Cho, Hosouk,Henry, William P.,Pittman, Jr., Charles U.

, p. 4188 - 4200 (2006)

Nucleophilic N-methyl cyclic ketene-N,X (X=S, O)-acetals can react with electrophilic aryl isocyanates and aryl isothiocyanates to form 'push-pull' mono-adducts, di-adducts and spirobicyclic 6/5 ring compounds.

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)

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.

-

Usanmaz

, p. 1117 (1979)

-

Method for preparing aromatic isocyanate terpolymer

-

Paragraph 0020; 0022; 0030-0031; 0033-0039, (2021/06/22)

The invention discloses a method for preparing an aromatic isocyanate terpolymer in the field of high polymer material synthesis, which comprises the following steps of S1, respectively taking dimethylacetamide, ethanol and sodium hydride, taking dimethylacetamide as a solvent, taking ethanol and sodium hydride as catalysts, adding into a flask, and reacting at room temperature, S2, dropwise adding aromatic isocyanate as a reaction substrate, and carrying out a heating reaction under magnetic stirring, S3, after the mixture is cooled to the room temperature, pouring the mixture into ultrapure water to separate out a product, filtering the product, washing the precipitate with water and ethanol in sequence, and drying the precipitate in a drying oven to obtain a crude product. According to the method, dimethylacetamide is used as a solvent, under the condition that ethanol is not changed, a small amount of sodium hydride is used for base catalysis of polymerization of aromatic isocyanate such as 3, 5-dimethyl phenyl isocyanate to synthesize the compound aromatic isocyanate tripolymer, the yield of the aromatic isocyanate tripolymer can be increased, the cost can be reduced, and use by people is facilitated.

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

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