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5-methoxy-2-n-octyl-N-(quinolin-8-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1428858-63-2

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1428858-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428858-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,8,5 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1428858-63:
(9*1)+(8*4)+(7*2)+(6*8)+(5*8)+(4*5)+(3*8)+(2*6)+(1*3)=202
202 % 10 = 2
So 1428858-63-2 is a valid CAS Registry Number.

1428858-63-2Downstream Products

1428858-63-2Relevant academic research and scientific papers

Nickela-electrocatalyzed Mild C?H Alkylations at Room Temperature

Ackermann, Lutz,Samanta, Ramesh C.,Struwe, Julia

supporting information, p. 14154 - 14159 (2020/06/17)

Direct alkylations of carboxylic acid derivatives are challenging and particularly nickel catalysis commonly requires high reaction temperatures and strong bases, translating into limited substrate scope. Herein, nickel-catalyzed C?H alkylations of unactivated 8-aminoquinoline amides have been realized under exceedingly mild conditions, namely at room temperature, with a mild base and a user-friendly electrochemical setup. This electrocatalyzed C?H alkylation displays high functional group tolerance and is applicable to both the primary and secondary alkylation. Based on detailed mechanistic studies, a nickel(II/III/I) catalytic manifold has been proposed.

Nickel-catalyzed direct alkylation of C-H bonds in benzamides and acrylamides with functionalized alkyl halides via bidentate-chelation assistance

Aihara, Yoshinori,Chatani, Naoto

supporting information, p. 5308 - 5311 (2013/05/21)

The alkylation of the ortho C-H bonds in benzamides and acrylamides containing an 8-aminoquinoline moiety as a bidentate directing group with unactivated alkyl halides using nickel complexes as catalysts is described. The reaction shows high functional group compatibility. In reactions of meta-substituted aromatic amides, the reaction proceeds in a highly selective manner at the less hindered C-H bond.

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