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((2S,3R)-3-Phenyl-oxiranyl)-thiophen-3-yl-methanone is a complex organic compound characterized by its unique molecular structure. It features a chiral center, with the 2S,3R configuration indicating that the hydroxyl group and the phenyl group are positioned on the same side of the molecule when viewed from the perspective of the chiral carbon. The compound consists of a phenyl-oxirane ring, which is a three-membered ring containing an oxygen atom, attached to a thiophene ring through a methylene bridge. The thiophene ring itself is a five-membered aromatic ring with one sulfur atom. ((2S,3R)-3-Phenyl-oxiranyl)-thiophen-3-yl-methanone is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structural features.

86022-38-0

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86022-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86022-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,2 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86022-38:
(7*8)+(6*6)+(5*0)+(4*2)+(3*2)+(2*3)+(1*8)=120
120 % 10 = 0
So 86022-38-0 is a valid CAS Registry Number.

86022-38-0Downstream Products

86022-38-0Relevant academic research and scientific papers

Synthetic Enzymes. Part 2. Catalytyc Asymmetric Epoxidation by means of Polyamino-acids in a Triphase System

Julia, Sebastian,Guixer, Joan,Masana, Jaume,Rocas, Jose

, p. 1317 - 1324 (2007/10/02)

The asymmetric epoxidation of several chalcones and other electron-poor olefins, in the presence of catalytic amounts of poly-(S)-amino-acids in a triphase system with optical yields of up to 96percent is described.The influence of the molecular structure of the catalysts and substrates, the solvent, and the temperature on the stereochemistry is discussed.

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