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1-(3-Ethylsulfanyl-propylamino)-3-(4-methoxy-phenoxy)-propan-2-ol is a complex organic compound with the molecular formula C15H25NO3S. It is characterized by a propane-2-ol backbone, which is a three-carbon alcohol with a hydroxyl group at the second carbon. The compound features a 3-ethylsulfanyl-propylamino group attached to the first carbon, which introduces a sulfur atom and a propyl chain with an ethylsulfanyl (ethylthio) group. On the third carbon, there is a 4-methoxy-phenoxy group, which consists of a phenyl ring with a methoxy (oxygen-carbon) substituent at the fourth position and an ether linkage to the propane-2-ol backbone. This chemical structure suggests potential applications in pharmaceuticals or as a precursor in the synthesis of other organic compounds, given its unique functional groups and structural features.

67215-01-4

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67215-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67215-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,1 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67215-01:
(7*6)+(6*7)+(5*2)+(4*1)+(3*5)+(2*0)+(1*1)=114
114 % 10 = 4
So 67215-01-4 is a valid CAS Registry Number.

67215-01-4Downstream Products

67215-01-4Relevant academic research and scientific papers

β-Adrenergic blocking agents. 18. 1-(Aryloxy)-3-(arylthioaklylamino)propan-2-ols and 1-substituted alkylthioamino-3-(aryloxy)propan-2-ols

Tucker,Coope

, p. 769 - 773 (2007/10/06)

The synthesis is described of a series of derivatives of 1-(aryloxy)-3-(arylthioalkylamino)propan-2-ols and 1-(alkylthioamino)- and 1-(aralkylamino)-3-(aryloxy)propan-2-ols. These compounds were investigated for their β-adrenoreceptor blocking properties and their selectivity of action for the cardiac β1 receptor. The structure-activity relationships are discussed with particular reference to the effects of the sulfur, sulfoxide, and sulfone groups on β-adrenoreceptor blocking potency and selectivity.

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