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N1,N3-bis(4,6-dichloro-1,3,5-triazin-2-yl)benzene-1,3-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13859-11-5

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13859-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13859-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,5 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13859-11:
(7*1)+(6*3)+(5*8)+(4*5)+(3*9)+(2*1)+(1*1)=115
115 % 10 = 5
So 13859-11-5 is a valid CAS Registry Number.

13859-11-5Relevant academic research and scientific papers

Evaluation of the binding ability of tetraaza[2]arene[2]triazine receptors anchoring l-alanine units for aromatic carboxylate anions

Vicente, Ana I.,Caio, Jo?o M.,Sardinha, Jo?o,Moiteiro, Cristina,Delgado, Rita,Félix, Vítor

, p. 670 - 680 (2012)

The binding affinities of three new tetraaza[2]arene[2]triazine based macrocycles anchoring one (AC1A) and two (AC2A and Me4AC2A) l-alanine amino acid units for five aromatic carboxylate anions (bz-, ph 2-, iph2-, tph2- and btc3-) were investigated in DMSO-d6. 1H NMR titrations revealed that the AC1A and AC2A receptors exhibit comparable anion affinities, suggesting that the two l-alanine binding units in AC2A are not simultaneously involved in the anion recognition as indicated by molecular dynamics simulations carried out for selected AC1A and AC2A associations using the AMBER force field (GAFF). New force field parameters were developed in order to mimic the structural singularity derived from the N-H macrocyclic bridges.

Synthesis and structure of a novel thiacalix[4]arene based triazine derivative

Deng, Min,Mu, Lan,Zeng, Xi,Jiang, Xue-Kai,Zhang, Yun-Qian,Yamato, Takehiko

, p. 512 - 514 (2013)

Using thiacalix[4]arene and 1,3-bis-(dichloro-s-triazinyloxy)benzene as a starting materials, a novel thiacalix[4]arene based triazine derivative has been designed and synthesized. This nucleophilic displacement reaction occurred in mild condition. The co

Excellent performance of aromatic polyguanamines induced by multiple hydrogen bondable tetraazacalix[2]arene[2]-triazine ring in their main chain

Sasaki,Kotaki,Fujimori,Tsukamoto,Suzuki,Oishi,Shibasaki

, p. 1361 - 1370 (2020/01/25)

A series of poly(guanamine) (c-PG)s containing tetraazacalix[2]arene[2]-triazine (mPDA2CyC2) were successfully prepared by solution polycondensation of mPDA2CyC2 with various aromatic diamines in an aprotic orga

NOVEL TRIAZINE DERIVATIVE AND PHOTOSENSITIVE COMPOSITION COMPRISING SAME

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Paragraph 0128, (2020/08/30)

The present invention relates to a compound represented by any one of the following formula A to formula C, and a photosensitive composition comprising the same, wherein the structure of the compound represented by any one of formula A to formula C is as described in the detailed description of the invention.

A general and high yielding fragment coupling synthesis of heteroatom-bridged calixarenes and the unprecedented examples of calixarene cavity fine-tuned by bridging heteroatoms

Wang, Mei-Xiang,Yang, Hai-Bo

, p. 15412 - 15422 (2007/10/03)

A number of aza- and/or oxo-bridged calix[2]arene[2]triazines have been synthesized through an unusually high yielding and efficient fragment coupling approach starting from cyanuric chloride and resorcinol, 3-aminophenol, m-phenylenediamine, and N,N-dime

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