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134856-57-8

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134856-57-8 Usage

triazen derivative

contains a diethyl group and a phenyl group with a trimethylsilyl ethynyl substituent

Chemical and pharmaceutical applications

used as a reagent in organic synthesis and as a precursor in the preparation of other organic compounds

Potential use

in the development of new pharmaceutical agents and in biological research

Unique structure and properties

valuable building block for the synthesis of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 134856-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,5 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134856-57:
(8*1)+(7*3)+(6*4)+(5*8)+(4*5)+(3*6)+(2*5)+(1*7)=148
148 % 10 = 8
So 134856-57-8 is a valid CAS Registry Number.

134856-57-8Relevant articles and documents

Symmetrically backfolded molecules emulating the self-similar features of a Sierpinski triangle

Hu, Jie-Ying,Sun, Yan-Qiong,Xiao, Ran,Cheng, Shengxian,He, Jun,Zeller, Matthias,Wong, Wai-Yeung,Xu, Zhengtao

, p. 6032 - 6037 (2019/06/24)

We synthesized self-similar molecules (G3 and G2; based on phenylalkynyl backbones) with symmetrically backfolded shapes inspired by the famous fractal of a Sierpinski triangle. Unlike the more traditional, starburst dendrimers, the centripetal-shaped Sierpinski molecules feature side branches symmetrically bent away from the growth direction of the main branch, thus contrasting the natural-tree shape. Molecule G3 exhibits three distinct levels of the structural hierarchy comprising the primary, secondary and tertiary branches, while the smaller G2 contains only features of the 1st and 2nd orders. In spite of the much larger conjugated backbone of G3, its solution UV-vis absorption and fluorescence exhibit no red shift relative to G2. In a test of nitrobenzene sensing, a thin film of G3 deposited from THF was more sensitively quenched in fluorescence than the smaller G2.

Rapid solution and solid phase synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5-thiopheneethynylene)]s

Li, Guorong,Wang, Xianhong,Li, Ji,Zhao, Xiaojiang,Wang, Fosong

, p. 2576 - 2582 (2007/10/03)

Monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5-thiopheneethynylene)] s, new candidates for molecular wires, were rapidly synthesized via an iterative divergent/convergent doubling strategy in solution as well as on Merrifield's resin.

Synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5- thiopheneethynylene)]s

Li, Guorong,Wang, Xianhong,Li, Ji,Zhao, Xiaojiang,Wang, Fosong

, p. 115 - 119 (2007/10/03)

The synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5- thioph-eneethynylene)]s using an iterative divergent/convergent doubling strategy based on Sonogashira coupling reaction was presented.

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