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2-[(methyl(phenylamino))methyl]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

151291-56-4

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151291-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151291-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 151291-56:
(8*1)+(7*5)+(6*1)+(5*2)+(4*9)+(3*1)+(2*5)+(1*6)=114
114 % 10 = 4
So 151291-56-4 is a valid CAS Registry Number.

151291-56-4Downstream Products

151291-56-4Relevant academic research and scientific papers

Cu-Catalyzed Cross-Dehydrogenative ortho-Aminomethylation of Phenols

Yu, Congjun,Patureau, Frederic W.

, p. 11807 - 11811 (2018)

A highly selective CuII-catalyzed cross-dehydrogenative ortho-aminomethylation of phenols with aniline derivatives is described. The corresponding C(sp2)?C(sp3) coupling products were obtained in moderate to excellent yields under mild reaction conditions and with a broad substrate scope. A radical mechanism is proposed.

Cr-Catalyzed Direct ortho-Aminomethylation of Phenols

Shi, Junbin,Wang, Yubin,Bu, Qingqing,Liu, Binyuan,Dai, Bin,Liu, Ning

, p. 17567 - 17580 (2021/12/17)

We developed a Cr-catalyzed strategy for the regioselective formation of Csp2–Csp3 bonds through the direct and efficient ortho-aminomethylation of N,N-dimethylanilines with phenols. The approach showed excellent site selectivity at the ortho-position of phenols and accommodated broad substrate scope and functional group compatibility for both N,N-dimethylanilines and phenols. Mechanistic studies revealed that the direct ortho-aminomethylation between N,N-dimethylanilines and phenols occurred via an ionic mechanism.

Nickel Catalyzed Ipso-hydroxylation and Subsequent Cross Dehydrogenative Coupling of Arylboronic Acids with Tertiary Amines: A Facile Access to α-phenolated Tertiary Amines

Kumar, Promod,Kumar Sharma, Anup,Singh, Rahul,Guntreddi, Tirumaleswararao,Nand Singh, Krishna

supporting information, p. 1786 - 1789 (2018/03/28)

A straightforward and new approach has been developed for the α-functionalization of tertiary amines via sequential oxidative hydoxylation and cross-dehydrogenative coupling (CDC) of arylboronic acids with tertiary amines to afford α-phenolated tertiary amines. The results demonstrate an easy arylation of C(sp3)?H bond in the presence of an inexpensive and readily available nickel metal salt. (Figure presented.).

Metal-Free Diaryl Etherification of Tertiary Amines by Ortho-C(sp2)-H Functionalization for Synthesis of Dibenzoxazepines and -ones

Jamsheena, Vellekkatt,Mahesha, Chikkagundagal K.,Joy, M. Nibin,Lankalapalli, Ravi S.

supporting information, p. 6614 - 6617 (2017/12/26)

A phenyliodine(III) diacetate mediated umpolung reactivity of the tertiary amines with suitably substituted o-hydroxybenzyl and phenyl groups is exploited to facilitate o-C(sp2)-H functionalization to afford diaryl ethers. The presence of an o-

Palladium-Catalyzed Regioselective C-Benzylation via a Rearrangement Reaction: Access to Benzyl-Substituted Anilines

Amézquita-Valencia, Manuel,Alper, Howard

, p. 16774 - 16778 (2016/11/17)

An unprecedented C-benzylation rearrangement reaction, catalyzed by palladium, is reported. The reaction proceeds by rearrangement leading to the direct synthesis of para or ortho benzyl-substituted N-methylanilines. The product is obtained in high regioselectivity, without the need to use a ligand for the catalytic process.

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