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2,5-bis[tolyl(hydroxy)methyl]thieno[3,2-b]thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1618679-28-9

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1618679-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1618679-28-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,8,6,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1618679-28:
(9*1)+(8*6)+(7*1)+(6*8)+(5*6)+(4*7)+(3*9)+(2*2)+(1*8)=209
209 % 10 = 9
So 1618679-28-9 is a valid CAS Registry Number.

1618679-28-9Downstream Products

1618679-28-9Relevant academic research and scientific papers

Aromatic Fused [30] Heteroannulenes with NIR Absorption and NIR Emission: Synthesis, Characterization, and Excited-State Dynamics

Mallick, Abhijit,Oh, Juwon,Kim, Dongho,Rath, Harapriya

, p. 8026 - 8031 (2016)

Two hitherto unknown planar aromatic [30] fused heterocyclic macrocycles (1.1.0.1.1.0), with NIR absorption in free-base form and protonation-induced enhanced NIR emission, have been synthesized from easy to make precursors. The induced correspondence of

Aromatic fused heterocyclic [22] macrocycles with NIR absorption

Rath, Harapriya,Mallick, Abhijit,Ghosh, Tubai,Kalita, Alok

, p. 9094 - 9096 (2014)

Three related aromatic [22] heteroporphyrins have been synthesized and characterized, with the target of achieving NIR absorption. The propensity of these smallest π-conjugated macrocycles to absorb in the NIR region is benefitted from the fusion/annelati

Protonation Dependent Topological Dichotomy of Core Modified Hexaphyrins: Synthesis, Characterization, and Excited State Dynamics

Mallick, Abhijit,Oh, Juwon,Majewski, Marcin A.,St?pień, Marcin,Kim, Dongho,Rath, Harapriya

, p. 556 - 566 (2017)

Two hitherto unknown core modified hexaphyrin analogues have been synthesized and characterized where the conformational dynamics of these macrocycles in the free base form is achieved by the rotation of thienothiophene units. Further unique property of t

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