57899-54-4 Usage
Uses
Used in Organic Synthesis:
1-Isopropoxycyclohexene is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules. Its cyclic ether structure and isopropoxy group make it a versatile building block in the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
1-Isopropoxycyclohexene is used as an intermediate in the synthesis of pharmaceutical compounds for its potential to form key structural elements in drug molecules. Its reactivity and stability under controlled conditions make it a valuable component in the development of new medications.
Used in Chemical Research:
1-Isopropoxycyclohexene is used as a model compound in chemical research to study the properties and reactivity of cyclic ethers. Understanding its behavior can provide insights into the broader class of ether compounds and their potential applications in various fields.
Used in Material Science:
1-Isopropoxycyclohexene is used as a precursor in the development of new materials, such as polymers and resins, for its potential to influence the properties of these materials. Its incorporation into the molecular structure can affect characteristics like strength, flexibility, and chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 57899-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,9 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57899-54:
(7*5)+(6*7)+(5*8)+(4*9)+(3*9)+(2*5)+(1*4)=194
194 % 10 = 4
So 57899-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-8(2)10-9-6-4-3-5-7-9/h6,8H,3-5,7H2,1-2H3
57899-54-4Relevant academic research and scientific papers
Production of secondaryalkoxy-1-alkenes
-
, (2008/06/13)
The present invention relates to a general synthesis for producing secondaryalkoxy-1-alkenes in commercial quantities in good yields by reacting cyclic and acyclic ketones and the corresponding alcohol with a secondary alkyl orthoformate ester in the presence of an acid catalyst, a Lewis acid, ferric chloride being preferred, and recovering the produce as a liquid of high purity.
An efficient synthesis of ketone enol ethers mediated by N-(1-alkoxyalkyl)benzotriazoles
Katritzky,Bayyuk,Rachwal
, p. 279 - 283 (2007/10/02)
A new general method for the transformation of ketones into their enol ethers in good yield is developed via elimination of benzotriazole from N-(1-alkoxyalkyl)benzotriazole intermediates.
