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1,2-cis-diphenoxyethylene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73421-47-3

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73421-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73421-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,2 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73421-47:
(7*7)+(6*3)+(5*4)+(4*2)+(3*1)+(2*4)+(1*7)=113
113 % 10 = 3
So 73421-47-3 is a valid CAS Registry Number.

73421-47-3Downstream Products

73421-47-3Relevant academic research and scientific papers

Highly Active Cross-Metathesis of Tetrafluoroethylene with a Seven-Membered N-Heterocyclic-Carbene-Ruthenium Catalyst

Mori, Kenta,Akiyama, Midori,Inada, Ko,Imamura, Yutaka,Ishibashi, Yuichiro,Takahira, Yusuke,Nozaki, Kyoko,Okazoe, Takashi

, p. 20980 - 20987 (2021/12/14)

A drastic increase in catalyst turnover number (TON) was accomplished in the cross-metathesis of tetrafluoroethylene (TFE) and vinyl ethers. Under a continuous flow of TFE, catalyst Ru7, which contains a seven-membered N-heterocyclic carbene (NHC) ligand, reached a TON of 4100; this is 2 orders of magnitude higher than the highest hitherto reported value. Mechanistic studies revealed that the expanded NHC successfully destabilizes the stable intermediates with a difluorocarbene structure, which strongly promotes the reaction.

Low energy light-triggered oxidative cleavage of olefins

Murthy, Rajesh S.,Bio, Moses,You, Youngjae

supporting information; experimental part, p. 1041 - 1044 (2009/05/27)

A series of substituted olefins were tested for their reactivity with singlet oxygen as a singlet oxygen-mediated cleavable linker. Low intensity light of 200 mW/cm2 was irradiated to the solution of an olefin and 5,10,15-triphenyl-20-(4-hydroxyphenyl)-21H,23H-porphyrin under atmospheric condition. Among the tested olefins, 1,2-cis-diphenoxyethylene reacted fast with singlet oxygen, >80% within 15 min yielding a stoichiometric conversion to aldehyde product without any side reactions.

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