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1-(morpholin-4-yl)-4-phenylbutane-1-thione is an organic compound with the molecular formula C16H21NOS2. It is a derivative of butane-1-thione, featuring a morpholine ring attached to the 1-position and a phenyl group at the 4-position. 1-(morpholin-4-yl)-4-phenylbutane-1-thione is characterized by its thioether and amine functional groups, which contribute to its unique chemical properties. It is typically used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form stable complexes with metal ions. The compound's structure allows for a range of applications, including its use in the development of chelating agents and as a building block for more complex organic molecules.

3657-94-1

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3657-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3657-94-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3657-94:
(6*3)+(5*6)+(4*5)+(3*7)+(2*9)+(1*4)=111
111 % 10 = 1
So 3657-94-1 is a valid CAS Registry Number.

3657-94-1Downstream Products

3657-94-1Relevant academic research and scientific papers

Silica-supported fluoroboric acid (HBF4-SiO2) catalyzed highly productive synthesis of thiomorpholides as activators of l-asparaginase as well as the antioxidant agent

Bandgar, Babasaheb P.,Gawande, Shrikant S.,Warangkar, Suchita C.,Totre, Jalinder V.

, p. 3618 - 3624 (2010)

An efficient solvent-free procedure for the synthesis of thiomorpholides in the presence of a catalytic amount of solid-supported fluoroboric acid (HBF4-SiO2) is described. The advantages of this method are high yields, short reaction times, ease of product isolation, low cost, and the catalyst can be recycled for a number of times without significant loss of activity. Three thiomorpholides possessing electron-donating group (4c, 4g, and 4h) were exhibiting excellent stimulatory activities against Erwinia carotovora l-asparaginase. The most potent activator, compound 4h displayed the following kinetic parameters, Km = 75 μM and Vmax = 1000 μmol mg-1 min-1 and KA = 0.985 μM. Furthermore, these compounds (4g, 4h, 4c, 4f, 4a, and 4d) have also shown promising 2,2′-diphenyl-1-picrylhydrazyl (DPPH) reducing antioxidant activity (21-36%) at 1 mM concentration as compared to standard butylated hydroxyl anisole (72% at 1 mM).

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