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N-(3-carbamoyl-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)-2-(5-methylfuran-2-yl)quinoline-4-carboxamide is a complex organic compound with a molecular formula of C23H20N2O4S2. This chemical is characterized by a quinoline-4-carboxamide core, which is substituted with a 5-methylfuran-2-yl group at the 2-position and a 3-carbamoyl-4,5,6,7-tetrahydro-1-benzothiophen-2-yl group at the N-position. The compound's structure features a benzothiophene ring fused to a tetrahydro ring, which is further connected to a quinoline ring through a carbamoyl linkage. This specific arrangement of functional groups and rings endows the molecule with unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

5700-37-8

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5700-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5700-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5700-37:
(6*5)+(5*7)+(4*0)+(3*0)+(2*3)+(1*7)=78
78 % 10 = 8
So 5700-37-8 is a valid CAS Registry Number.

5700-37-8Downstream Products

5700-37-8Relevant academic research and scientific papers

Dehydrogenative Coupling of Hydrosilanes and Alcohols by Alkali Metal Catalysts for Facile Synthesis of Silyl Ethers

Harinath, Adimulam,Bhattacharjee, Jayeeta,Anga, Srinivas,Panda, Tarun K.

, p. 724 - 730 (2017/05/31)

Cross-dehydrogenative coupling (CDC) of hydrosilanes with hydroxyl groups, using alkali metal hexamethyldisilazide as a single-component catalyst for the formation of Si-O bonds under mild condition, is reported. The potassium salt [KN(SiMe3)2] is highly efficient and chemoselective for a wide range of functionalized alcohols (99% conversion) under solvent-free conditions. The CDC reaction of alcohols with silanes exhibits first-order kinetics with respect to both catalyst and substrate concentrations. The most plausible mechanism for this reaction suggests that the initial step most likely involves the formation of an alkoxide followed by the formation of metal hydride as active species.

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