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Triphenyl(phenylethynyl)phosphonium is a phosphonium compound characterized by its chemical formula C32H25P. It is a colorless crystalline solid that is soluble in organic solvents. triphenyl(phenylethynyl)phosphonium is formed by the combination of three phenyl groups attached to a phosphorus atom and a phenylethynyl group, which is an ethynyl group (C≡CH) attached to a phenyl ring. Triphenyl(phenylethynyl)phosphonium is often used as a reagent in organic synthesis, particularly in the formation of carbon-carbon triple bonds through the Sonogashira coupling reaction. It is also employed in the synthesis of various organic compounds and materials, such as conductive polymers and pharmaceuticals. Due to its unique structure and reactivity, it plays a significant role in the field of organic chemistry and materials science.

34387-64-9

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34387-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34387-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34387-64:
(7*3)+(6*4)+(5*3)+(4*8)+(3*7)+(2*6)+(1*4)=129
129 % 10 = 9
So 34387-64-9 is a valid CAS Registry Number.

34387-64-9Relevant academic research and scientific papers

HSP70 INHIBITORS AND METHODS OF USING SAME

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Page/Page column 67-68, (2021/10/11)

The disclosure provides compounds, and compositions comprising such compounds, that can be used to treat cancer, especially colorectal cancer (CRC). In certain embodiments, the compounds of the disclosure inhibit HSP70. In other embodiments, the compounds of the disclosure promote or increase immune cell recruitment to a cancer. In yet other embodiments, the compounds of the disclosure promote or increase immune cell infiltration in a cancer.

A reinvestigation of mono-and bis-ethynyl phosphonium salts: Structural and computational studies and new reactivity

Veinot, Alex J.,Todd, Angela D.K.,Robertson, Katherine N.,Masuda, Jason D.

, p. 8 - 17 (2018/01/17)

A series of mono-and bis-ethynyl phosphonium salts have been prepared via reaction of bromoacetylenes, Ph-C≡C-Br or Br-C≡C-C6H4-C≡C-Br, with various phosphines. Some of the derivatives reported are previously known, ([Ph-C≡C-PPh3]Br, [Ph-C≡C-PMe3]Br, [Ph-C≡C-PBu3]Br, and [Ph3P-C≡C-C6H4-C≡C-PPh3][Br2]), however typically these are missing complete spectroscopic characterization and many have been prepared using much more complicated methods. The derivative [Ph-C≡C-PPh3]Br is capable of inhibiting the growth of tumour cells and has been shown crystallographically to have a significant interaction with the heat shock proteins (HSP70 or DnaK). Thus, solid state structures for all seven phosphonium salts prepared have been reported as they may be of interest to others in this field. Sterically encumbered phosphines such as Mes3P did not react with Ph-C≡C-Br; however, (2,4,6-MeO-C6H2)3P was found to slowly react at moderate temperature to give the expected alkynyl phosphonium salt. However, at higher temperatures, the alkynyl phosphonium undergoes an intramolecular cyclization to form a phosphonium analogue of a 1,4-oxazine. Finally, electronic structure calculations reveal the positive charge on the acetylenic β-carbon, a result of a significant contribution of other canonical structures. The flexibility of the P-C≡C bond has been investigated showing a low-energy barrier (3]+ cation. This ease of bending may be of significance in the development of other alkynyl phosphonium tumour cell growth inhibitors.

Ethynylphosphonium Salts, 2. A New Method for the Preparation of Ethynyltriphenylphosphonium Salts

Bestmann, Hans Juergen,Kisielowski, Lothar

, p. 1320 - 1326 (2007/10/02)

The reaction between substituted (benzoylmethylene)- and (carbamoylmethylene)triphenylphosphoranes and the adduct of bromine to triphenylphosphane in the presence of triethylamine gives rise to the formation of (phenylethynyl)- resp. (aminoethynyl)triphen

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