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1,3-Benzenedicarboxylic acid, 5-(1,1-dimethylethyl)-, diethyl ester, also known as diethyl 5-tert-pentylphthalate or DEHP, is a colorless, odorless liquid with the chemical formula C20H30O4. It is a widely used plasticizer, primarily in the production of flexible polyvinyl chloride (PVC) products such as films, sheets, tubes, and cables. DEHP enhances the flexibility, durability, and workability of PVC materials, making it an essential component in various industries, including automotive, construction, and medical. However, concerns have been raised about its potential health and environmental impacts, as it can leach out of PVC products and has been classified as a possible human carcinogen by some regulatory agencies. As a result, there is ongoing research and development of alternative plasticizers to replace DEHP in certain applications.

64148-47-6

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64148-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64148-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,4 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64148-47:
(7*6)+(6*4)+(5*1)+(4*4)+(3*8)+(2*4)+(1*7)=126
126 % 10 = 6
So 64148-47-6 is a valid CAS Registry Number.

64148-47-6Downstream Products

64148-47-6Relevant academic research and scientific papers

Synthesis and structures of NCN pincer-type ruthenium and iridium complexes bearing protic pyrazole arms

Toda, Tatsuro,Saitoh, Koki,Yoshinari, Akihiro,Ikariya, Takao,Kuwata, Shigeki

, p. 1188 - 1195 (2017)

The reaction of the 1,3-bis(pyrazol-3-yl)-benzenes 1 with [RuCl(OAc)(PPh3)3] resulted in selective C-H cleavage at the 2-position of 1 to give the protic NCN pincer-type ruthenium(II) complexes [RuCl(R-NCN-LH2)-(PPh3)2] (2; R-NCN-LH2 = 4-R-2,6-bis(5-tert-butyl-1H-pyrazol-3-yl)phenyl). Similar cyclometalation with iridium trichloride followed by addition of triphenylphosphine led to the formation of the iridium(III) analogue [IrCl(But-NCN-LH2)(PPh3)]Cl (5). Treatment of the ruthenium complexes 2 with carbon monoxide afforded the carbonyl complexes [Ru(CO)(R-NCN-LH2)(PPh3)2]Cl (4). On the other hand, the pyridine analogue of 1, 2,6-bis(5-tert-butyl-1H-pyrazol-3-yl)pyridine (NNN-LH2), reacted with iridium trichloride to yield the protic NNN pincer-type complex [IrCl3(NNN-LH3)] (7)., 2,6-bis(5-tert-butyl-1H-pyrazol-3-yl)pyridine (NNN-LH2), reacted with iridium trichloride to yield the protic NNN pincer-type complex [IrCl3(NNN-LH3)] (7).. The stronger ω donation of the NCN pincer-type ligand in comparison with the analogous NNN ligand was suggested by the CO stretching frequencies of the ruthenium carbonyl complexes 4 as well as the M-Cl distances. The catalytic activity of the ruthenium complexes 2a,b toward transfer hydrogenation of a ketone was also evaluated.

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