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4-chlorophenyl(2,4-dimethoxypyrimidin-5-yl)ketone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1201670-62-3

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1201670-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201670-62-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,7 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1201670-62:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*7)+(3*0)+(2*6)+(1*2)=103
103 % 10 = 3
So 1201670-62-3 is a valid CAS Registry Number.

1201670-62-3Downstream Products

1201670-62-3Relevant academic research and scientific papers

Deprotonative metalation of aromatic compounds by using an amino-based lithium cuprate

Nguyen, Tan Tai,Marquise, Nada,Chevallier, Floris,Mongin, Florence

experimental part, p. 10405 - 10416 (2011/10/12)

Deprotonative cupration of aromatic compounds by using amino-based lithium cuprates was optimized with 2,4-dimethoxypyrimidine and 2-methoxypyridine as the substrates and benzoyl chloride as the electrophile. [(tmp)2CuLi] (+2 LiCl) (tmp=2,2,6,6-tetramethylpiperidino) was identified as the best reagent and its use was extended to anisole, 1,4-dimethoxybenzene, other substituted pyridines, furan, thiophene and derivatives, and N-Boc-indole (Boc=tert-butyloxycarbonyl). Of the electrophiles employed to attempt the interception of the generated aryl cuprates, aroyl chlorides, iodomethane, and diphenyl disulfide efficiently reacted. In addition, different oxidative agents were identified to afford symmetrical biaryls. Finally, palladium-catalyzed coupling with aryl halides was optimized and allowed the synthesis of different aryl derivatives in medium to good yields.

New Gilman-type lithium cuprate from a copper(II) salt: synthesis and deprotonative cupration of aromatics

Nguyen, Tan Tai,Chevallier, Floris,Jouikov, Viatcheslav,Mongin, Florence

experimental part, p. 6787 - 6790 (2010/04/29)

Deprotonative cupration of aromatics including heterocycles (anisole, 1,4-dimethoxybenzene, thiophene, furan, 2-fluoropyridine, 2-chloropyridine, 2-bromopyridine, and 2,4-dimethoxypyrimidine) was realized in tetrahydrofuran at room temperature using the Gilman-type amido-cuprate (TMP)2CuLi in situ prepared from CuCl2·TMEDA through successive addition of 1 equiv of butyllithium and 2 equiv of LiTMP. The intermediate lithium (hetero)arylcuprates were evidenced by trapping with iodine, allyl bromide, methyl iodide, and benzoyl chlorides, the latter giving the best results. Symmetrical dimers were also prepared from lithium azine and diazine cuprates using nitrobenzene as an oxidative agent.

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