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Thiophene, 2,2'-[oxybis(methylene)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35250-78-3

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35250-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35250-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,5 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35250-78:
(7*3)+(6*5)+(5*2)+(4*5)+(3*0)+(2*7)+(1*8)=103
103 % 10 = 3
So 35250-78-3 is a valid CAS Registry Number.

35250-78-3Downstream Products

35250-78-3Relevant academic research and scientific papers

Palladium-catalyzed N-alkylation of amides and amines with alcohols employing the aerobic relay race methodology

Yu, Xiaochun,Jiang, Lan,Li, Qiang,Xu, Qing,Xie, Yuanyuan

, p. 2322 - 2332,11 (2012)

Possibly because homogeneous palladium catalysts are not typical borrowing hydrogen catalysts and ligands are thus ineffective in catalyst activation under conventional anaerobic conditions, they had not been used in the N-alkylation reactions of amines/amides with alcohols in the past. By employing the aerobic relay race methodology with Pd-catalyzed aerobic alcohol oxidation being a more effective protocol for alcohol activation, ligand-free homogeneous palladiums are successfully used as active catalysts in the dehydrative N-alkylation reactions, giving high yields and selectivities of the alkylated amides and amines. Mechanistic studies implied that the reaction most probably proceeds via the novel relay race mechanism we recently discovered and proposed. By employing the aerobic relay race methodology with Pd-catalyzed aerobic alcohol oxidation being a more effective protocol for alcohol activation, ligand-free homogeneous palladiums are successfully used as active catalysts in the dehydrative N-alkylation reactions of amines and amides with alcohols, giving high yields and selectivities of the alkylated amines and amides. Mechanistic studies implied that the reaction most probably proceeds via the novel relay race mechanism we recently discovered and proposed. Copyright

Photochemical reactions of Thienyl-, Bithienyl-, Terthienyl- and Thienylaroyl-methanols

Krishnaswamy, N. R.,Kumar, Ch. Siva Sai Kamana,Prasanna, S.

, p. 1801 - 1830 (2007/10/02)

Photochemical reactions of some thienyl-, bithienyl-, terthienyl- and thienylaroyl-methanols were studied in the neat state as well as in solvents like methanol and benzene.The terthienylmethanols were found to be susceptible to photo-sensitized oxidation which was inhibited by singlet oxygen quenchers.The photoproducts were isolated, characterised by spectroscopic methods and in some cases by synthesis.

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