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1-ethynyl-2-((2-vinylphenyl)ethynyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1048972-22-0

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1048972-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1048972-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,8,9,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1048972-22:
(9*1)+(8*0)+(7*4)+(6*8)+(5*9)+(4*7)+(3*2)+(2*2)+(1*2)=170
170 % 10 = 0
So 1048972-22-0 is a valid CAS Registry Number.

1048972-22-0Downstream Products

1048972-22-0Relevant academic research and scientific papers

Systematic investigation of silver-carbon bonding in coordination frameworks with aryl ligands that contain ethynyl and ethenyl substituents

Hau, Sam C. K.,Mak, Thomas C. W.

, p. 5387 - 5400 (2013)

Single-crystal X-ray diffraction of a series of ten crystalline silver(I)-trifluoroacetate complexes that contained designed ligands, each of which was composed of an aromatic system that was functionalized with terminal and internal ethynyl groups and a

Radical cascade transformations of tris(o-aryleneethynylenes) into substituted benzo[a]indeno[2,1-c]fluorenes

Alabugin, Igor V.,Gilmore, Kerry,Patil, Satish,Manoharan, Mariappan,Kovalenko, Serguei V.,Clark, Ronald J.,Ghiviriga, Ion

supporting information; experimental part, p. 11535 - 11545 (2009/02/03)

Oligomeric o-aryleneethynylenes with three triple bonds undergo cascade radical transformations in reaction with a Bu3SnH/AIBN system. These cascades involve three consecutive cycle closures with the formation of substituted benzo[a]indeno[2,1-c]fluorene or benzo[1,2]fluoreno[4,3-b]silole derivatives. The success of this sequence depends on regioselectivity of the initial attack of the Bu3Sn radical at the central triple bond of the o-aryleneethynylene moiety. The cascade is propagated through the sequence of 5-exo-dig and 6-exo-dig cyclizations which is followed by either a radical attack at the terminal Ar substituent or radical transposition which involves H-abstraction from the terminal TMS group and 5-endo-trig cyclization. Overall, the transformation has potential to be developed into an approach to a new type of graphite ribbons.

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