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Benzoic acid, 4,4'-[(6-chloro-1,3,5-triazine-2,4-diyl)diimino]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61981-57-5

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61981-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61981-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,8 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61981-57:
(7*6)+(6*1)+(5*9)+(4*8)+(3*1)+(2*5)+(1*7)=145
145 % 10 = 5
So 61981-57-5 is a valid CAS Registry Number.

61981-57-5SDS

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 4-[[4-(4-carboxyanilino)-6-chloro-1,3,5-triazin-2-yl]amino]benzoic acid

1.2 Other means of identification

Product number -
Other names 4,4'-[(6-chloro-1,3,5-triazine-2,4-diyl)diimino]bis-benzoic acid

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:61981-57-5 SDS

61981-57-5Relevant academic research and scientific papers

Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation

Funfuenha, Watcharee,Phakhodee, Wong,Pattarawarapan, Mookda

, p. 5415 - 5419 (2014)

A rapid and efficient method for preparation of C2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks.

Complexes of iron(III) and chromium(III) salen and salophen Schiff bases with bridging 1,3,5-triazine derived multidirectional ligands

Koc, Ziya Erdem

experimental part, p. 769 - 775 (2011/10/04)

Figure represented. A new synthetic route for preparing multidirectional ligands was developed by using 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) as core. The reaction included the selective substitutions of 4-aminobenzoic acid onto three chlorides of the triazine ring via a stepwise manner at 1:1, 1:2, or 1:3 equiv. and 0, 25, 130°C, respectively. An efficient synthesis of a novel class of "multidirectional ligands" has been developed based on high-yielding chloride substitutions of 2,4,6-trichloro-1,3,5-triazine by amines. Sixteen new mono-, di-, tri-, and tetra-nuclear Fe(III) and Cr(III) complexes involving tetradenta Schiff bases N,N′-bis(salicylidene)ethylenediamine-(salenH2) or bis(salicylidene)-o-phenylenediamine-(salophenH2) with two new 1,3,5-triazine derived multidirectional ligands were synthesized and characterized by means of elemental analysis, 1H NMR, FT-IR spectroscopy, LC-MS analysis, AAS, thermal analysis, and magnetic susceptibility measurements. The complexes were also characterized as low-spin distorted octahedral Fe(III) and Cr(III) bridged by carboxylic acids. It was understood that the [{Fe(salen)/(salophen)}2O] and [{Cr(salen)/(salophen)} 2O] containing compounds could be represented by the electronic structure of t2g5eg0 and t 2g3eg0.

An efficient, "green" approach to aryl amination of cyanuric chloride using acetic acid as solvent

Kolmakov, Kirill A.

, p. 533 - 539 (2008/09/18)

(Chemical Equation Presented) Acetic acid is an inexpensive and environmentally friendly solvent for facile, clean and high-yielding aryl amination of cyanuric chloride with aromatic amines, including nitroanilines. Aryl animation in acetic acid medium and isolation protocol are greatly simplified as compared to previously reported procedures. Under proper conditions, it is possible to attach the same or different aniline residues in a controlled way to obtain in excellent yields symmetrical and unsymmetrical 1,3,5-triazine derivatives, respectively.

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