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N(CH2C5H4N)2CH2C5H3NN(CH2C6H5)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1023595-98-3

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1023595-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1023595-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,3,5,9 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1023595-98:
(9*1)+(8*0)+(7*2)+(6*3)+(5*5)+(4*9)+(3*5)+(2*9)+(1*8)=143
143 % 10 = 3
So 1023595-98-3 is a valid CAS Registry Number.

1023595-98-3Relevant academic research and scientific papers

Amine oxidative N-dealkylation via cupric hydroperoxide Cu-OOH homolytic cleavage followed by site-specific fenton chemistry

Kim, Sunghee,Ginsbach, Jake W.,Lee, Jung Yoon,Peterson, Ryan L.,Liu, Jeffrey J.,Siegler, Maxime A.,Sarjeant, Amy A.,Solomon, Edward I.,Karlin, Kenneth D.

, p. 2867 - 2874 (2015/03/14)

Copper(II) hydroperoxide species are significant intermediates in processes such as fuel cells and (bio)chemical oxidations, all involving stepwise reduction of molecular oxygen. We previously reported a CuII-OOH species that performs oxidative N-dealkylation on a dibenzylamino group that is appended to the 6-position of a pyridyl donor of a tripodal tetradentate ligand. To obtain insights into the mechanism of this process, reaction kinetics and products were determined employing ligand substrates with various para-substituent dibenzyl pairs (-H,-H; -H,-Cl; -H,-OMe, and -Cl,-OMe), or with partially or fully deuterated dibenzyl N-(CH2Ph)2 moieties. A series of ligand-copper(II) bis-perchlorate complexes were synthesized, characterized, and the X-ray structures of the -H,-OMe analogue were determined. The corresponding metastable CuII-OOH species were generated by addition of H2O2/base in acetone at -90 °C. These convert (t1/2 ≈ 53 s) to oxidatively N-dealkylated products, producing para-substituted benzaldehydes. Based on the experimental observations and supporting DFT calculations, a reaction mechanism involving dibenzylamine H-atom abstraction or electron-transfer oxidation by the CuII-OOH entity could be ruled out. It is concluded that the chemistry proceeds by rate limiting Cu-O homolytic cleavage of the CuII-(OOH) species, followed by site-specific copper Fenton chemistry. As a process of broad interest in copper as well as iron oxidative (bio)chemistries, a detailed computational analysis was performed, indicating that a CuIOOH species undergoes O-O homolytic cleavage to yield a hydroxyl radical and CuIIOH rather than heterolytic cleavage to yield water and a CuII-O?- species.

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