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2,3,6,7-tetrakis(4-bromophenyl)benzo[lmn][2,9]phenanthroline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403336-90-2

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1403336-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403336-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,3,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1403336-90:
(9*1)+(8*4)+(7*0)+(6*3)+(5*3)+(4*3)+(3*6)+(2*9)+(1*0)=122
122 % 10 = 2
So 1403336-90-2 is a valid CAS Registry Number.

1403336-90-2Downstream Products

1403336-90-2Relevant academic research and scientific papers

Concise synthesis and two-photon-excited deep-blue emission of 1,8-diazapyrenes

He, Tingchao,Too, Pei Chui,Chen, Rui,Chiba, Shunsuke,Sun, Handong

, p. 2090 - 2095 (2012/10/30)

Efficient violet-blue-emitting molecules are especially useful for applications in full-color displays, solid-state lighting, as well as in two-photon absorption (TPA) excited frequency-upconverted violet-blue lasing. However, the reported violet-blue-emitting molecules generally possess small TPA cross sections. In this work, new 1,8-diazapyrenes derivatives 3 with blue two-photon-excited fluorescence emission were concisely synthesized by the coupling reaction of readily available 1,4-naphthoquinone O,O-diacetyl dioxime (1) with internal alkynes 2 under the [{RhCl2Cp*} 2]-Cu(OAc)2 (Cp=pentamethylcyclopentadienyl ligand) bimetallic catalytic system. Elongation of the π-conjugated length of 1,8-diazapyrenes 3 led to the increase of TPA cross sections without the expense of a redshift of the emission wavelength, probably due to the rigid planar structure of chromophores. It is especially noteworthy that 2,3,6,7-tetra(4- bromophenyl)-1,8-diazapyrene (3 c) has a larger TPA cross section than those of other molecules reported so far. These experimental results are explained in terms of the effects of extension of the π-conjugated system, intramolecular charge transfer, and reduced detuning energy. Copyright

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