176-91-0 Usage
Cyclic organic compound
1-Oxaspiro[4.5]decane is a cyclic compound, meaning its carbon atoms form a closed loop or ring.
Unique structure
1-Oxaspiro[4.5]decane has a specific arrangement of atoms that differentiates it from other organic compounds, giving it potential as a building block for synthesis.
Building block for synthesis
Due to its unique structure, 1-Oxaspiro[4.5]decane can be used as a starting point for creating other organic compounds through chemical reactions.
Solvent properties
1-Oxaspiro[4.5]decane can dissolve other substances, making it useful as a solvent in various chemical processes.
Production of fragrances and flavors
The compound is used in the creation of scented and flavored products, likely due to its own distinctive odor and taste properties.
Valuable component in industrial and chemical processes
The unique structure and properties of 1-Oxaspiro[4.5]decane make it an important ingredient in a variety of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 176-91-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 176-91:
(5*1)+(4*7)+(3*6)+(2*9)+(1*1)=70
70 % 10 = 0
So 176-91-0 is a valid CAS Registry Number.
176-91-0Relevant articles and documents
Trianion synthon approach to spirocyclic heterocycles
Perry, Matthew A.,Hill, Richard R.,Rychnovsky, Scott D.
supporting information, p. 2226 - 2229 (2013/06/05)
A variety of spirocyclic heterocycles have been constructed by a double-alkylation and reductive cyclization approach utilizing α-heteroatom nitriles as trianion synthons. The method provides access to heteroatom-substituted spirocycles in a variety of ring sizes that are found in natural products and are important in pharmaceutical lead development and optimization.
γ-Lithioalkoxides via Reductive Lithiation of Oxetanes by Aromatic Radical Anions
Mudryk, Boguslaw,Cohen, Theodore
, p. 5657 - 5659 (2007/10/02)
Oxetanes are cleaved at 0 deg C in tetrahydrofuran by lithium 4,4'-di-tert-butylbiphenylide, giving lithium γ-lithioalkoxides which can provide 2-substituted tetrahydrofurans by trapping with aldehydes and ketones followed by acid cyclization of the resulting 1,4-diols; the cuprates of these dianions undergo conjugate addition and nucleophilic substitution reactions.
Direct synthesis of Ethers via Zinc Chloride Mediated Etherification of Alcohols in Dichloroethane
Kim, Sunggak,Chung, Ki Nam,Yang, Sungbong
, p. 3917 - 3919 (2007/10/02)
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