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Trifluoromethyl-5 phenylthio-2 phenylamine is a complex organic compound characterized by its unique molecular structure. It features a trifluoromethyl group (-CF3), a phenylthio group (-SPh), and two phenylamine groups (-NHPh). trifluoromethyl-5 phenylthio-2 phenylamine is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its reactivity and stability. The presence of the trifluoromethyl group imparts lipophilicity and metabolic stability, which are desirable properties in drug design. The phenylthio and phenylamine moieties contribute to the compound's electronic and steric properties, influencing its interactions with biological targets. Overall, trifluoromethyl-5 phenylthio-2 phenylamine is a versatile building block in organic synthesis, with its properties making it a candidate for further exploration in the development of new chemical entities.

52548-94-4

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52548-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52548-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,4 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52548-94:
(7*5)+(6*2)+(5*5)+(4*4)+(3*8)+(2*9)+(1*4)=134
134 % 10 = 4
So 52548-94-4 is a valid CAS Registry Number.

52548-94-4Relevant academic research and scientific papers

Note on Unusual Behaviour of 2,3,4,5-Tetrahydro-1,5-benzothiazepin-4-ones During Arylation

Ried, Walter,Sell, Gunther

, p. 1913 - 1916 (2007/10/02)

The 5-aryl-2,3,4,5-tetrahydro-1,5-benzothiazepines 3a-c have been synthesized by arylation of the corresponding 2,3,4,5-tetrahydro-1,5-benzothiazepin-4-ones 1.However, in some of these reactions the diaryl sulfides 4a,b and 5 were formed.

10,11-Dihydro-dibenzo(b,f)thiepin derivatives

-

, (2016/03/01)

Dibenzothiepin derivatives of the general formula STR1 wherein m, n, R1, R2, R3 and X are as hereinafter set forth, And salts thereof as well as processes for their manufacture are disclosed. The end products are useful as central-depressant and neuroleptic agents.

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