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1,3,5-tris(4-nitrophenyl)-1,3,5-triazinane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7507-66-6

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7507-66-6 Usage

Type of compound

Triazine derivative

Common uses

a. Organic synthesis
b. Building block for functional materials

Properties

a. Strong electron-withdrawing due to 4-nitrophenyl groups
b. Enhanced electronic properties

Applications

a. Materials science
b. Organic electronics
c. Pharmaceuticals

Safety precautions

Proper handling and safety measures required due to potentially hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 7507-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7507-66:
(6*7)+(5*5)+(4*0)+(3*7)+(2*6)+(1*6)=106
106 % 10 = 6
So 7507-66-6 is a valid CAS Registry Number.

7507-66-6SDS

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-nitrophenyl)-1,3,5-triazinane

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:7507-66-6 SDS

7507-66-6Relevant academic research and scientific papers

Novel reaction of N,N′-bisarylmethanediamines with formaldehyde. Synthesis of some new 1,3,5-triaryl-1,3,5-hexahydrotriazines

Ghandi, Mehdi,Salimi, Farshid,Olyaei, Abolfazl

, p. 556 - 563 (2006)

The acid-catalyzed cyclocondensation of N,N′-bisaryl (aryl = 2-pyrimidinyl, 2-pyrazinyl and 4-nitrophenyl) methanediamines 5a-c with aqueous formaldehyde in refluxing acetonitrile leads to the formation of the corresponding 1,3,5-triaryl-1,3,5-hexahydrotr

Synthesis of α-Amino Tertiary Alkylperoxides by Lewis Acid-Catalyzed Peroxidation of 1,3,5-Triazines

Liu, Lijuan,Shi, Zhichao,Zhang, Xun,Zhan, Feng,Lin, Jin-Shun,Jiang, Yuyang

supporting information, p. 3487 - 3491 (2021/09/20)

α-Substituted peroxides have been found in natural products and are widely used as anti-malarial agents. Zn(OTf)2-catalyzed peroxidation of 1,3,5-triazines has been developed, accessing diversely substituted α-amino tertiary alkylperoxides with high efficiency. Mechanistic investigations and useful synthetic application of the products have also been presented.

Ultrasound-assisted synthesis of substituted triazines and their corrosion inhibition behavior on N80 steel/acid interface

Salman, Mohammad,Ansari, Kashif R.,Haque, Jiyaul,Srivastava, Vandana,Quraishi, Mumtaz A.,Mazumder, Mohammad A. J.

, p. 2157 - 2172 (2020/03/04)

The three substituted triazines were synthesized by ultrasound irradiation method and characterized by FTIR, 13C NMR, and 1H NMR. The corrosion inhibition behavior of the synthesized inhibitors on N80 steel in 15% HCl was studied using electrochemical analyses and weight loss methods. All three inhibitors exhibited excellent corrosion inhibition performance, and the best inhibition effect was shown by TZ-3 (93.2% at 800 mg/L). EIS measurements suggest that the corrosion inhibition process is a charge transfer controlled. The PDP results indicated that all the triazines are mixed-type inhibitors. Langmuir adsorption model is the best fit among the other tested isotherms. These molecules can act as promising acidizing corrosion inhibitors for the oil gas industry. FTIR, AFM, and UV-vis studies corroborate the adsorption of inhibitor molecules over the metal surface.

Synthesis of N-substituted 1,3,5-triazacyclohexanes catalyzed by starch sulfuric acid

Wu, Hui,Yuan, Rui,Wan, Yu,Yin, Wei,Pang, Li-Ling

experimental part, p. 1097 - 1102 (2012/03/11)

N-substituted 1,3,5-triazacyclohexanes were simply synthesized from the reaction of aromatic or fatty amines and formaldehyde catalyzed by recyclable starch sulfuric acid with good yields at room temperature.

5-Substituted 2-alkyl- and 2-arylsulfonyliminohexahydro-1,3,5-triazines

Mel'nikova,Shagaeva,Luk'yanov

, p. 480 - 483 (2007/10/03)

A new procedure was developed for the preparation of previously unknown 5-substituted 2-alkyl- and 2-arylsulfonyliminohexahydro-1,3,5-triazines by cyclocondensation of sulfoguanidines with formaldehyde and primary alkyl(aryl)amines.

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