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4-methylphenyl 5-(trifluoromethyl)-2-pyridinyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353258-10-3

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353258-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353258-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,5 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 353258-10:
(8*3)+(7*5)+(6*3)+(5*2)+(4*5)+(3*8)+(2*1)+(1*0)=133
133 % 10 = 3
So 353258-10-3 is a valid CAS Registry Number.

353258-10-3Downstream Products

353258-10-3Relevant academic research and scientific papers

Synthesis of Chiral Sulfoxides via Pd(II)-Catalyzed Enantioselective C-H Alkynylation/Kinetic Resolution of 2-(Arylsulfinyl)pyridines

Zhou, Tao,Jiang, Meng-Xue,Qian, Pu-Fan,Yao, Qi-Jun,Xu, Xue-Tao,Zhang, Kun,Shi, Bing-Feng

supporting information, p. 7910 - 7915 (2021/10/20)

A Pd(II)-catalyzed enantioselective C-H alkynylation of 2-(arylsulfinyl)pyridines via kinetic resolution using cheap and commercially available l-pGlu-OH as a chiral ligand is reported. A wide range of 2-(arylsulfinyl)pyridines were compatible with this p

Synthesis of Pyridylsulfonium Salts and Their Application in the Formation of Functionalized Bipyridines

Duong, Vincent K.,Horan, Alexandra M.,McGarrigle, Eoghan M.

supporting information, p. 8451 - 8457 (2020/11/12)

An S-selective arylation of pyridylsulfides with good functional group tolerance was developed. To demonstrate synthetic utility, the resulting pyridylsulfonium salts were used in a scalable transition-metal-free coupling protocol, yielding functionalized bipyridines with extensive functional group tolerance. This modular methodology permits selective introduction of functional groups from commercially available pyridyl halides, furnishing symmetrical and unsymmetrical 2,2′- A nd 2,3′-bipyridines. Iterative application of the methodology enabled the synthesis of a functionalized terpyridine with three different pyridine components.

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