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2-(2-methyl-6-phenethylphenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1261287-69-7

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1261287-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1261287-69-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,2,8 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1261287-69:
(9*1)+(8*2)+(7*6)+(6*1)+(5*2)+(4*8)+(3*7)+(2*6)+(1*9)=157
157 % 10 = 7
So 1261287-69-7 is a valid CAS Registry Number.

1261287-69-7Downstream Products

1261287-69-7Relevant academic research and scientific papers

Cobalt-Catalyzed Direct C(sp2)–H Alkylation with Unactivated Alkenes

Kim, Ye Lim,Park, Sun-a,Kim, Ju Hyun

supporting information, p. 4026 - 4030 (2020/06/17)

A facile and efficient method for Cp*CoIII-catalyzed C(sp2)–H bond alkylation was developed using 2-aryl pyridines and unactivated alkenes. The reaction proceeded atom-economically with readily available styrene derivatives and an ab

Ruthenium-catalyzed ortho-selective aromatic CH alkenylation with alkenyl carbonates

Ogiwara, Yohei,Kochi, Takuya,Kakiuchi, Fumitoshi

supporting information, p. 667 - 669 (2014/05/20)

Ortho-selective aromatic CH alkenylation with alkenyl carbonates proceeds in the presence of a catalytic amount of [Ru(cod)(cot)]. Arylpyridines and an aryloxazoline were regioselectively alkenylated without adding external bases. Aromatic CH alkylation also occurs depending on the reaction conditions.

Mild palladium-catalyzed C-H alkylation using potassium alkyltrifluoroborates in combination with MnF3

Neufeldt, Sharon R.,Seigerman, Cydney K.,Sanford, Melanie S.

supporting information, p. 2302 - 2305 (2013/06/05)

A Pd-catalyzed method for ligand-directed C-H alkylation with organoboron reagents is described. The combination of potassium organotrifluoroborates, MnF3, and a PdII catalyst effects pyridine and amide-directed C-H alkylation. These reactions proceed under mild conditions (25-40 C in weakly acidic media), are effective for installing methyl and 1 alkyl groups, and do not require promoters such as benzoquinone.

Regioselectivity-switchable hydroarylation of styrenes

Gao, Ke,Yoshikai, Naohiko

supporting information; experimental part, p. 400 - 402 (2011/04/16)

Cobalt-phosphine and cobalt-carbene catalysts have been developed for the hydroarylation of styrenes via chelationassisted C-H bond activation, to afford branched and linear addition products, respectively, in a highly regioselective fashion. Deuterium-la

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