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4-tert-butyl-N-methyl-N-phenylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70019-98-6

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70019-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70019-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,1 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70019-98:
(7*7)+(6*0)+(5*0)+(4*1)+(3*9)+(2*9)+(1*8)=106
106 % 10 = 6
So 70019-98-6 is a valid CAS Registry Number.

70019-98-6Relevant academic research and scientific papers

Nickel-Catalyzed Oxidative Transamidation of Tertiary Aromatic Amines with N -Acylsaccharins

Liu, Shengzhang,Yang, Lingyun,Tao, Jiasi,Yu, Weijie,Wang, Tao,Fu, Junkai

supporting information, p. 1642 - 1646 (2021/06/21)

The use of tertiary amines as surrogates for secondary amines has prominent advantages in terms of stabilization and ease of handling. A Ni-catalyzed transamidation of N -acylsaccharins with tertiary aromatic amines is reported. By using tert -butyl hydroperoxide as the terminal oxidant, this reaction permits selective cleavage of the C(sp 3)-N bonds of unsymmetrical tertiary aromatic amines depending on the sizes of the alkyl substituents.

N-Heterocyclic Carbene/Cobalt Cooperative Catalysis for the Chemo- and Regioselective C?N Bond Formation between Aldehyde and Amines/Amides

Siddiqui, Asher M.,Khalid, Anam,Khan, Arif,Azad, Chandra S.,Samim, Mohd.,Khan, Imran A.

, p. 4281 - 4287 (2020/07/24)

A novel methodology for the construction of various secondary (4 examples), tertiary amides (31 examples), and imides (16 examples) by a Cobalt(II) catalyzed oxidative amide coupling in aqueous media. The Co(III)-TMC was reacted with N-Heteroatom Carbene to form active catalyst Co(II)NHC-TMC in situ which involves in the coordination with Breslow's intermediate and SET for the activation of aldehyde and amides. The mechanism for activation of amide and amine differs on the basis of SET based nucleophilic addition and ligand exchange respectively. The regeneration of the catalyst was achieved using Fe(III)(EDTA)-H2O2 as oxidant. The use of Co(II)TMC-O2 was also found equally efficient in the process. The method is found regioselective for N?H activation in the presence of equally susceptible ortho-C?H bond activation. And amines were found more susceptible then the corresponding amide for the reaction.

NBu4NI-catalyzed unexpected amide bond formation between aldehydes and aromatic tertiary amines

Mai, Wen-Peng,Song, Ge,Yuan, Jin-Wei,Yang, Liang-Ru,Sun, Gang-Chun,Xiao, Yong-Mei,Mao, Pu,Qu, Ling-Bo

, p. 3869 - 3872 (2013/04/24)

A novel and practical amide bond formation method has been developed without the need for any metals. This method provides a novel route for amide bond formation, in the presence of an nBu4NI/TBHP catalyst system, from readily available aldehydes and aromatic tertiary amines.

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