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[2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol is a complex chemical compound characterized by its unique spiroketal structure, featuring a spiro carbon with two oxygen atoms attached. [2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol also includes four methyl groups and a hydroxyl group, contributing to its high level of steric complexity. The specific arrangement of atoms, with the stereochemistry indicated by the (S) designation, endows the compound with distinct properties and potential pharmaceutical applications. Its intricate structure and stereochemistry make it a fascinating subject for chemical synthesis and drug development research.

57967-71-2

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57967-71-2 Usage

Uses

Used in Pharmaceutical Applications:
[2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol is used as a pharmaceutical compound for its potential therapeutic applications. [2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol's unique structure and stereochemistry allow it to interact with biological targets in novel ways, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Chemical Synthesis Research:
[2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol is also used as a subject of study in chemical synthesis research. Its complex structure and stereochemistry present challenges and opportunities for scientists to develop new synthetic methods and strategies, potentially leading to the discovery of other complex and biologically active molecules.
Used in Drug Development Research:
[2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol is utilized in drug development research due to its potential to serve as a lead compound for the creation of new medications. [2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol's unique properties and interactions with biological systems make it an attractive starting point for the design and optimization of new therapeutic agents.
Used in Stereochemistry Studies:
[2alpha,5beta(S)]-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol is also used in stereochemistry studies to understand the impact of stereochemistry on the biological activity and pharmacokinetics of molecules. The (S) designation in its structure highlights the importance of stereochemistry in determining the compound's properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 57967-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,6 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57967-71:
(7*5)+(6*7)+(5*9)+(4*6)+(3*7)+(2*7)+(1*1)=182
182 % 10 = 2
So 57967-71-2 is a valid CAS Registry Number.

57967-71-2Downstream Products

57967-71-2Relevant academic research and scientific papers

Esters of certain tetramethyl and pentamethyl-1-oxa-spiro [4-5] decan-6-ols with certain alkanoic acids

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, (2008/06/13)

Spirane derivatives, most of them are new, useful as odor-modifying ingredients for manufacturing perfumes and perfumed products, and as flavor-modifying ingredients for the manufacture of artificial flavors of for flavoring foodstuffs, animal feeds, beverages, pharmaceutical preparations and tobacco products. Process for preparing said spirane derivatives.

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