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1,3-Bis[(2-bromo)benzene]triazene (HL) is a triazenido compound synthesized from 2-bromoaniline and sodium nitrite. It exhibits high selectivity for silver(I) ions over other metal ions, making it a potential candidate for silver ion detection or coordination chemistry applications. 1,3-bis[(2-bromo)benzene]triazene can form binuclear silver complexes, further highlighting its affinity for silver(I). No further relevant details are provided in the abstract.

70551-63-2

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70551-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70551-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,5 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70551-63:
(7*7)+(6*0)+(5*5)+(4*5)+(3*1)+(2*6)+(1*3)=112
112 % 10 = 2
So 70551-63-2 is a valid CAS Registry Number.

70551-63-2Upstream product

70551-63-2Relevant academic research and scientific papers

Synthesis and properties of 1,3-bis[(2-bromo)benzene]triazene and its binuclear silver complex

Xie, Qian-Ya,Liu, Wei-Xia,Zhan, Shu-Zhong,Wei, Xiao-Lan

, p. 630 - 636 (2020)

The reaction of 2-bromoaniline with sodium nitrite affords a triazenido compound, 1,3-bis[(2-bromo)benzene]triazene (HL). Spectroscopic investigations show that HL bears a high selectivity for silver(I) ion in the presence of other metal ions. In the pres

Synthesis and properties of amphiphilic photoresponsive gelators for aromatic solvents

Rajaganesh, Ramanathan,Gopal, Anesh,Mohan Das, Thangamuthu,Ajayaghosh, Ayyappanpillai

supporting information; experimental part, p. 748 - 751 (2012/03/26)

A sugar-based photoresponsive supergelator, N-glycosylazobenzene that shows selective gelation of aromatic solvents is described. The partial trans - cis isomerization of the azobenzene moiety allows photoinduced chopping of the entangled gel fibers to short fibers, resulting in controlled fiber length and gel - sol transition. The gelator is useful for the selective removal of toxic aromatic solvents from water.

A ligand-free copper (1) catalysed intramolecular N-arylation of diazoaminobenzenes in PEG-water: An expeditious protocol towards regiospecific 1-aryl benzotriazoles

Mukhopadhyay, Chhanda,Tapaswi, Pradip Kumar,Butcher, Ray J.

supporting information; experimental part, p. 4720 - 4729 (2010/11/17)

An efficient and highly versatile method for the synthesis of diverse regiospecific 1-arylbenzotriazoles being important medicinal scaffolds, by the copper (1) catalysed intramolecular N-arylation of diazoaminobenzenes of 2-haloaryldiazonium salts in PEG-water has been developed. A very simple reaction protocol, large number of substrate affordability and excellent yields are the main features of this methodology.

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