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N-(2-methoxy-4-methylphenyl)pivalamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74510-40-0

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74510-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74510-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74510-40:
(7*7)+(6*4)+(5*5)+(4*1)+(3*0)+(2*4)+(1*0)=110
110 % 10 = 0
So 74510-40-0 is a valid CAS Registry Number.

74510-40-0Relevant academic research and scientific papers

Remote amide-directed palladium-catalyzed benzylic C-H amination with N-fluorobenzenesulfonimide

Xiong, Tao,Li, Yan,Lv, Yunhe,Zhang, Qian

supporting information; experimental part, p. 6831 - 6833 (2010/10/21)

An unprecedented remote amide-directed palladium-catalyzed intermolecular highly selective benzylic C-H amination with N-fluorobenzenesulfonimide is developed, which represents the first direct benzylic C-H amination with a non-nitrene nitrogen source. This methodology provides a novel approach to circumvent the common ortho aromatic C-H selectivity in directed palladium catalyzed C-H functionalization.

A brief and convergent synthetic route to defucogilvocarcin M chromophore: The formal synthesis of WS-5995 A and C

Patra, Asit,Pahari, Pallab,Ray, Sutapa,Mal, Dipakranjan

, p. 9017 - 9020 (2007/10/03)

Densely substituted styryl sulfone 20 is shown to undergo double annulation with phthalide 21 to give, in one-pot operation and in excellent yield, the benzonaphthopyranone scaffold 22 of gilvocarcins.

Synthesis of The Gilvocarcin-M Aglycone

McKenzie, Thomas C.,Hassen, Wesley,Macdonald, Simon J. F.

, p. 5435 - 5436 (2007/10/02)

The synthesis of the aglycone of the antibiotic Gilvocarcin-M by a sequential Meerwein Diels-Alder route is reported.The D-ring of the aglycone is attached by a halogen atom directed Meerwein arylation reaction and the A-ring is attached by a halogen atom directed Diels-Alder reaction.In the key step the directing chlorine atom is removed by a new thiophenylation reduction sequence.

Synthesis of maytansinoids: the aromatic moiety of maytansine

Ho, Pak-Tsun

, p. 861 - 863 (2007/10/02)

A simple and novel synthesis of the tetrasubstituted aromatic compound related to the "western-southern" region of maytansine has been achieved.

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