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(4-(phenylbuta-1,3-diyn-1-yl)phenyl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1416169-75-9

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1416169-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416169-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,1,6 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1416169-75:
(9*1)+(8*4)+(7*1)+(6*6)+(5*1)+(4*6)+(3*9)+(2*7)+(1*5)=159
159 % 10 = 9
So 1416169-75-9 is a valid CAS Registry Number.

1416169-75-9Relevant academic research and scientific papers

A sensitive and specific Raman probe based on bisarylbutadiyne for live cell imaging of mitochondria

Yamakoshi, Hiroyuki,Palonpon, Almar,Dodo, Kosuke,Ando, Jun,Kawata, Satoshi,Fujita, Katsumasa,Sodeoka, Mikiko

, p. 664 - 667 (2015)

We previously showed that bisarylbutadiyne (BADY), which has a conjugated diyne structure, exhibits an intense peak in the cellular Raman-silent region. Here, we synthesized a mitochondria-selective Raman probe by linking bisphenylbutadiyne with triphenylphosphonium, a well-known mitochondrial targeting moiety. This probe, named MitoBADY, has a Raman peak 27 times more intense than that of 5-ethynyl-2′-deoxyuridine. Raman microscopy using submicromolar extracellular probe concentrations successfully visualized mitochondria in living cells. A full Raman spectrum is acquired at each pixel of the scanned sample, and we showed that simultaneous Raman imaging of MitoBADY and endogenous cellular biomolecules can be achieved in a single scan. MitoBADY should be useful for the study of mitochondrial dynamics.

In the optically-multiplexed-

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Paragraph 0216, (2020/12/30)

A method for optical super-multiplexing using polyynes to provide enhanced images from stimulated Raman microscopy is disclosed. In some exemplary embodiments, the polyynes are organelle-targeted or spectral barcoded. Imaging can be enhanced by using the polyynes to image whole live cells or specific organelles within live cells. The polyynes can also be used in optical data storage (i.e., encoding) and identification (i.e., decoding) applications.

Application of polymer microspheres to Raman detection

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Paragraph 0135; 0148-0150, (2018/03/13)

The invention discloses application of polymer microspheres to Raman detection. Methacrylate/amide polymer monomers or styrene polymer monomers containing alkynyl, cyano, azido or a carbon-deuterium bond group are prepared into the polymer microspheres with the particle diameter from a nanometer grade to a micron grade through an emulsion polymerization or dispersion polymerization method; the polymer microspheres have a remarkable Raman signal under the condition of no metal sensitization structure; and a Raman characteristic peak signal is located in a Raman quiet zone (1800cm to 2800cm) in a living organism and can be used as a marker for biological imaging.

Optimization of solid-supported Glaser-Hay reactions in the microwave

Lampkowski, Jessica S.,Maza, Johnathan C.,Verma, Sanjana,Young, Douglas D.

, p. 5276 - 5285 (2015/05/13)

The translation of organometallic reactions into a microwave reactor has numerous advantages. Herein, we describe the application of a previously developed solid-supported Glaser-Hay reaction to microwave conditions. Overall, an array of diynes has been prepared demonstrating the ability to conduct chemoselective reactions in the microwave within 20 min compared to the 16 h thermal conditions. Moreover, non-microwave transparent alkynes have been found to react more quickly, preventing catalyst quenching, and resulting in higher yields.

Development of solid-supported Glaser-Hay couplings

Tripp, Valerie T.,Lampkowski, Jessica S.,Tyler, Ryan,Young, Douglas D.

supporting information, p. 164 - 167 (2014/05/06)

While the Glaser-Hay coupling of terminal alkynes is a useful reaction, several issues associated with chemoselectivity preclude its widespread application in synthetic chemistry. To address these issues, a solid-supported Glaser-Hay methodology was developed to afford only asymmetric diyne products. This methodology was then applied to a series of immobilized alkynes with a diverse set of soluble alkynes to generate an array of heterocoupled products in high yields and purities.

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