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The chemical compound "((2R,4aR)-7-Oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-phenyl-trimethylsilanyloxy-acetonitrile" is a complex organic molecule with a unique structure. It features a naphthalene-based core, which is a type of polycyclic aromatic hydrocarbon, with an octahydro substitution pattern, indicating that it has eight hydrogen atoms attached to the carbon framework. The molecule also includes a phenyl group, which is a benzene ring, and a trimethylsilanyloxy group, suggesting the presence of a silicon atom bonded to three methyl groups and an oxygen atom. Additionally, it contains an acetonitrile moiety, which is a cyano group (CN) attached to an acetone-like structure. ((2R,4aR)-7-Oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-phenyl-trimethylsilanyloxy-acetonitrile is characterized by its stereochemistry, with the 2R,4aR configuration indicating the specific three-dimensional arrangement of atoms around the asymmetric carbon centers. Overall, ((2R,4aR)-7-Oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-phenyl-trimethylsilanyloxy-acetonitrile is a sophisticated example of organic chemistry, with potential applications in various fields such as pharmaceuticals, materials science, or as a synthetic intermediate.

73593-55-2

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73593-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73593-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,9 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73593-55:
(7*7)+(6*3)+(5*5)+(4*9)+(3*3)+(2*5)+(1*5)=152
152 % 10 = 2
So 73593-55-2 is a valid CAS Registry Number.

73593-55-2Downstream Products

73593-55-2Relevant academic research and scientific papers

Trimethylsilyl Cyanide - A Reagent for Umpolung, III: Nucleophilic Acylation of α,β-Unsaturated Carbonyl Compounds with directed 1,2-/1,4-Additions by Solvent Effects

Huenig, Siegfried,Wehner, Gregor

, p. 302 - 323 (2007/10/02)

The anion 7 of O-(trimethylsilyl)cyanohydrine 6, derived from benzaldehyde, attacks numerous α-enones in ether exclusively by 1,4-addition, even if C-3 is alkyl-substituted.In THF and DME the 1,2-adduct is formed predominantly; on addition of HMPT or 12-c

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