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1-(3-Ethylsulfanyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol is a complex organic compound with the molecular formula C13H20N2O4S. It features a propane-2-ol backbone, with a 3-ethylsulfanyl-propylamino group attached to the first carbon and a 2-nitro-phenoxy group attached to the third carbon. The presence of the nitro group (-NO2) on the phenoxy ring and the sulfanyl group (-SH) on the propylamine chain contribute to its unique chemical properties. 1-(3-Ethylsulfanyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol may have potential applications in pharmaceuticals or chemical research due to its diverse functional groups, although specific uses would depend on further investigation into its properties and reactivity.

56215-59-9

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56215-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56215-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,1 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56215-59:
(7*5)+(6*6)+(5*2)+(4*1)+(3*5)+(2*5)+(1*9)=119
119 % 10 = 9
So 56215-59-9 is a valid CAS Registry Number.

56215-59-9Downstream Products

56215-59-9Relevant 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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