22094-00-4 Usage
Uses
Used in Flavor and Fragrance Industry:
1-Ethoxy-3-methyl-2-butene is used as a flavoring agent for its ester-like, fruity odor. It is particularly suitable for enhancing the aroma of various food products, such as beverages, confectionery, and baked goods, due to its pleasant and recognizable scent.
Used in Perfumery:
In the perfumery industry, 1-ethoxy-3-methyl-2-butene is used as a fragrance ingredient. Its fruity and ester-like odor contributes to the creation of various perfume compositions, adding a fresh and appealing note to the overall scent.
Used in Chemical Synthesis:
1-Ethoxy-3-methyl-2-butene can also be utilized as a starting material or intermediate in the synthesis of other organic compounds. Its unique structure allows for further chemical reactions, leading to the production of various chemicals with different applications in the pharmaceutical, agrochemical, and other specialty chemical industries.
Used in Research and Development:
Due to its distinctive chemical properties, 1-ethoxy-3-methyl-2-butene is often employed in research and development settings. It serves as a valuable compound for studying various chemical reactions, mechanisms, and processes, contributing to the advancement of scientific knowledge in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 22094-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22094-00:
(7*2)+(6*2)+(5*0)+(4*9)+(3*4)+(2*0)+(1*0)=74
74 % 10 = 4
So 22094-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O/c1-4-8-6-5-7(2)3/h5H,4,6H2,1-3H3
22094-00-4Relevant academic research and scientific papers
Reaction of orthoesters with alcohols in the presence of acidic catalysts: A study
Sampath Kumar,Joyasawal, Sipak,Reddy,Pawan Chakravarthy,Krishna,Yadav
, p. 1686 - 1692 (2007/10/03)
Allylic and benzylic alcohols are converted into corresponding unsymmetrical ethers when reacted with various orthoesters in the presence of montmorillonite KSF at ambient temperature. A detailed study has been undertaken to examine the mechanism and generality of these reactions with regard to various acidic catalysts, which reveal interesting competitive reactions mainly O-acetylation, together with trace amount of dimerized product. The type of the side product and their relative quantity depends upon the nature of the catalyst employed. Furthermore, the low yields of the Claisen rearrangement product obtained from allylic alcohols under heating is rationalized due to the formation of some of these products.
