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"7,11,18,21-tetraoxa-trispiro[5.2.2.5.2.2]heneicosane" is a complex organic compound characterized by its unique molecular structure. It consists of three spiro-linked rings, each formed by five carbon atoms, with an additional oxygen atom incorporated into the structure at the 7th, 11th, 18th, and 21st positions. 7,11,18,21-tetraoxa-trispiro[5.2.2.5.2.2]heneicosane is a member of the spiro compound family, which are known for their cyclic structures that twist around a common center. The presence of oxygen atoms in the molecule suggests potential applications in various chemical industries, such as the synthesis of surfactants or as intermediates in the production of other complex organic molecules. The specific arrangement of atoms and the spiro structure contribute to its distinct chemical properties and potential reactivity, making it a subject of interest for researchers in organic chemistry.

183-10-8

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183-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183-10-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 183-10:
(5*1)+(4*8)+(3*3)+(2*1)+(1*0)=48
48 % 10 = 8
So 183-10-8 is a valid CAS Registry Number.

183-10-8Downstream Products

183-10-8Relevant academic research and scientific papers

A Facile, Selective Preparation of Monoketals from Pentaerythritol and Ketones

Murguia, Marcelo C.,Vaillard, Santiago E.,Grau, Ricardo J.

, p. 1093 - 1097 (2001)

The selective preparation of monoketals 3a-f from pentaerythritol 1 and cyclic, acyclic, aromatic, and aliphatic ketones 2a-f was achieved by a facile method. The extreme polarity and low solubility of pentaerythritol in almost all organic solvents were the main difficulties to be overcome for the preparation of monoketals in good yields and high selectivity. A benzene-dimethylformamide (40:60) mixture proved to be excellent for the ketalization. The one-step procedure developed allowed the preparation of monoketals in good yields and good to excellent selectivity (higher than 90 percent).

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