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1-(2-bromo-4-trifluoromethyl-phenyl)-ethanol is an organic compound with the molecular formula C8H7BrF3O. It features a phenyl ring substituted with a bromine atom at the 2nd position and a trifluoromethyl group at the 4th position. The ethanol moiety is attached to the 1st position of the phenyl ring, making it a phenylethanol derivative. 1-(2-bromo-4-trifluoromethyl-phenyl)-ethanol is characterized by its unique combination of functional groups, which may contribute to its potential applications in various chemical and pharmaceutical industries. Due to its halogenated and fluorinated nature, it could be used as an intermediate in the synthesis of more complex molecules or as a reagent in organic reactions.

349-68-8

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349-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349-68-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 349-68:
(5*3)+(4*4)+(3*9)+(2*6)+(1*8)=78
78 % 10 = 8
So 349-68-8 is a valid CAS Registry Number.

349-68-8Relevant academic research and scientific papers

PdII-Catalyzed Oxidative Tandem aza-Wacker/Heck Cyclization for the Construction of Fused 5,6-Bicyclic N,O-Heterocycles

Ye, Chenghao,Kou, Xuezhen,Xia, Jingzhao,Yang, Guoqiang,Kong, Li,Wei, Quhao,Zhang, Wanbin

supporting information, p. 1897 - 1901 (2018/07/31)

A PdII-catalyzed oxidative tandem cyclization was developed for the construction of fused 5,6-bicyclic N, O-heterocycles. This reaction was enabled by the combined use of a 3-methylpyridine ligand and pentafluorobenzoic acid additive. A range of heterocyclic products with different substituents could be prepared in moderate to good yields via this methodology. Several transformations, including a scaled-up preparation of product 2 a, were also carried out showing the good applicability of our methodology.

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