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((2S,3R)-2-Ethyl-3-phenethyl-oxiranyl)-phenyl-methanone is a complex organic compound characterized by its chiral center, which gives it a specific three-dimensional arrangement. This molecule features a phenyl group (a benzene ring) attached to a methanone group, which is a carbonyl group (C=O) bonded to a methyl group. The oxirane ring, also known as an epoxide, is a three-membered ring consisting of two carbon atoms and one oxygen atom. The 2-ethyl and 3-phenethyl substituents on the oxirane ring further define its structure, with the ethyl group attached to the 2-position and the phenethyl group (a phenyl-ethyl group) attached to the 3-position. The stereochemistry at these positions is specified as (2S,3R), indicating the specific orientation of these substituents in space. ((2S,3R)-2-Ethyl-3-phenethyl-oxiranyl)-phenyl-methanone is of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structural features.

78844-14-1

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78844-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78844-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78844-14:
(7*7)+(6*8)+(5*8)+(4*4)+(3*4)+(2*1)+(1*4)=171
171 % 10 = 1
So 78844-14-1 is a valid CAS Registry Number.

78844-14-1Downstream Products

78844-14-1Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF α,β-EPOXYPHENYLKETONES FROM α,α-DIBROMOPHENYLKETONES AND ALDEHYDES USING STANNOUS FLUORIDE

Shoda, Shin-ichiro,Mukaiyama, Teruaki

, p. 723 - 724 (2007/10/02)

trans-α,β-Epoxyphenylketones are stereoselectively synthesized via aldol type intermediates under mild conditions starting from α,α-dibromophenylketones and aldehydes using stannous fluoride.

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