24469-79-2 Usage
Description
(E)-4-Hepten-1-ol, also known as phebalenol, is a chemical compound belonging to the alcohol family. It is a colorless liquid with a floral, green, and fatty odor, and is commonly utilized as a fragrance ingredient in the perfumery and personal care industries. (E)-4-Hepten-1-ol can be found naturally in various plants and contributes significantly to the aroma of certain fruits and vegetables. Its applications extend beyond the realm of fragrances, as it is also employed in the production of flavors, serves as a solvent in chemical reactions, and has been investigated for potential pharmaceutical uses and as a flavoring agent in the food industry.
Uses
Used in Perfumery and Personal Care Industry:
(E)-4-Hepten-1-ol is used as a fragrance ingredient for its floral, green, and fatty odor, adding a pleasant and natural scent to perfumes and other personal care products.
Used in Flavor Production:
(E)-4-Hepten-1-ol is used as a key component in the production of flavors, enhancing the aroma of certain fruits and vegetables, and contributing to the overall sensory experience of these products.
Used in Chemical Reactions as a Solvent:
(E)-4-Hepten-1-ol serves as a solvent in various chemical reactions, facilitating the process and improving the efficiency of these reactions.
Used in Pharmaceutical Research:
(E)-4-Hepten-1-ol is being studied for its potential use in the pharmaceutical industry, indicating its possible role in the development of new medications or therapeutic applications.
Used in the Food Industry as a Flavoring Agent:
(E)-4-Hepten-1-ol is also utilized as a flavoring agent in the food industry, where it helps to create and enhance the taste and aroma of various food products.
Check Digit Verification of cas no
The CAS Registry Mumber 24469-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,6 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24469-79:
(7*2)+(6*4)+(5*4)+(4*6)+(3*9)+(2*7)+(1*9)=132
132 % 10 = 2
So 24469-79-2 is a valid CAS Registry Number.
24469-79-2Relevant articles and documents
Access to Saturated Thiocyano-Containing Azaheterocycles via Selenide-Catalyzed Regio-A nd Stereoselective Thiocyanoaminocyclization of Alkenes
Wei, Wei,Liao, Lihao,Qin, Tian,Zhao, Xiaodan
, p. 7846 - 7850 (2019/10/10)
An efficient route for the synthesis of saturated thiocyano-containing azaheterocycles by selenide-catalyzed regio-A nd stereoselective thiocyanoaminocyclization of alkenes is disclosed. The desired products were obtained in moderate to high yields under mild conditions. The generality of this method was elucidated by its efficient application in thiocyano oxycyclization of alkenes.
Ring Scission Of Cyclic β-Halogeno-ethers with Samarium Di-iodide: A Synthesis of (E)- and (Z)-Enynols
Crombie, Leslie,Rainbow, Linda J.
, p. 6517 - 6520 (2007/10/02)
The use of samarium di-iodide in place of sodium metal for the ring scission of cyclic β-halogeno-ethers drastically alters the stereochemistry of the resulting olefinic alcohols: using the method, highly stereoselective syntheses of enynols in (Z)- and (E)-forms are reported.
RETENTION OF CONFIGURATION IN DOUBLE BOND PROTECTION-DEPROTECTION BY BROMINATION-CATHODIC DEBROMINATION
Husstedt, Urda,Schaefer, Hans J.
, p. 623 - 624 (2007/10/02)
The double bond can be mildly protected by bromination with PyHBr3; deprotection is achieved by cathodic reduction at -1.4 V.The overall yields range from 68 to 99 percent, the configuration of the double bond is retained with at least 96 percent.
