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1,4-bis(4-phenoxyphenyl)buta-1,3-diyne is a complex organic compound characterized by a buta-1,3-diyne backbone, which consists of a four-carbon chain with triple bonds between the first and second carbon atoms, and the third and fourth carbon atoms. The molecule features two phenoxyphenyl groups attached to the first and fourth carbon atoms of the buta-1,3-diyne chain. Each phenoxyphenyl group contains a phenyl ring (a six-carbon aromatic ring) and a phenoxy group (an oxygen atom bonded to a phenyl ring). 1,4-bis(4-phenoxyphenyl)buta-1,3-diyne is known for its unique electronic properties and potential applications in materials science, particularly in the development of organic semiconductors and optoelectronic devices. Its structure allows for π-conjugation, which is essential for charge transport and light absorption, making it a promising candidate for further research and development in these fields.

4200-17-3

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4200-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4200-17-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4200-17:
(6*4)+(5*2)+(4*0)+(3*0)+(2*1)+(1*7)=43
43 % 10 = 3
So 4200-17-3 is a valid CAS Registry Number.

4200-17-3Downstream Products

4200-17-3Relevant academic research and scientific papers

Functionalization of graphene oxide sheets with magnetite nanoparticles for the adsorption of copper ions and investigation of its potential catalytic activity toward the homocoupling of alkynes under green conditions

Baouab, Mohammed Hassen V.,Beyou, Emmanuel,Chaabane, Laroussi,Luneau, Dominique

, p. 91 - 103 (2020/05/29)

This paper deals with the preparation of graphene oxide sheets (GO) modified with magnetite nanoparticles (Fe3O4NPs) for removing Cu(II) ions from aqueous solutions. Moreover, the recovered Cu(II)-based material was recycled as a cat

Copper-Mediated Deacylative Coupling of Ynones via C-C Bond Activation under Mild Conditions

Feng, Lili,Hu, Tingjun,Zhang, Saisai,Xiong, Heng-Ying,Zhang, Guangwu

supporting information, p. 9487 - 9492 (2019/12/02)

The intermolecular deacylative coupling of unstrained ynones via C-C bond activation was accomplished by a CuCl-bpy system under mild reaction conditions. This protocol features facile cleavage of the C-C bond at room temperature, broad substrate scope, and efficient construction of important symmetric and unsymmetrical 1,3-diyne adducts through homo or cross coupling of ynones, respectively. The preliminary mechanistic investigations indicated that an acyl copper(III) complex is likely involved in this process.

Synthesis, structure and catalytic properties of [Ru(dppp) 2(CH3CN)Cl][BPh4] and isolation of catalytically active [Ru(dppp)2Cl][BPh4]: Ruthenium catalysed alkyne homocoupling and tandem alkyne-azide

Das, Uttam Kumar,Jena, Rajesh K.,Bhattacharjee, Manish

, p. 21964 - 21970 (2014/06/23)

The compound, [Ru(dppp)2(CH3CN)Cl][BPh4] (1) has been synthesised from the precursor complex, [Ru(PPh3) 3Cl2]. The complex has been structurally characterised. The complex has been found to

The oxygen-mediated synthesis of 1,3-butadiynes in continuous flow: Using teflon AF-2400 to effect gas/liquid contact

Petersen, Trine P.,Polyzos, Anastasios,O'Brien, Matthew,Ulven, Trond,Baxendale, Ian R.,Ley, Steven V.

supporting information; scheme or table, p. 274 - 277 (2012/05/05)

The gas is always greener: A continuous flow Glaser-Hay coupling reaction system, mediated by molecular oxygen, is developed based on a tube-in-tube gas/liquid reactor/injector. The system uses a semi-permeable Teflon AF-2400 membrane to effect rapid gas/

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