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2-(2-Bromo-phenylsulfanyl)-5-trifluoromethyl-phenylamine is a complex organic chemical compound characterized by its unique molecular structure. It features a phenylamine core, which is a derivative of aniline, with a bromine atom attached to the phenyl ring at the ortho position (2-position). Additionally, a trifluoromethyl group is present at the para position (5-position) of the phenylamine ring. The molecule also contains a sulfanyl group, which is a sulfur analog of a hydroxyl group, attached to the same phenyl ring as the bromine atom. 2-(2-Bromo-phenylsulfanyl)-5-trifluoromethyl-phenylamine is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its diverse functional groups and potential reactivity.

328-14-3

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328-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328-14-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 328-14:
(5*3)+(4*2)+(3*8)+(2*1)+(1*4)=53
53 % 10 = 3
So 328-14-3 is a valid CAS Registry Number.

328-14-3Relevant academic research and scientific papers

Assembly of substituted phenothiazines by a sequentially controlled CuI/L-proline-catalyzed cascade C-S and C-N bond formation

Dawei, Ma.,Geng, Qian,Zhang, Hui,Jiang, Yongwen

supporting information; experimental part, p. 1291 - 1294 (2010/05/17)

(Chemical equation presented) In the pro-line of fire: A general and efficient cascade reaction approach to substituted phenothiazines, which relies on controlled sequential Cul/L-prolinecatalyzed C-S and C-N bond formations, is described. DMSO = dimethylsulfoxide.

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