1223611-91-3 Usage
Description
1-(4-fluorophenyl)buta-2,3-dien-1-one, also known as 4-Fluorocinnamaldehyde, is a chemical compound characterized by its molecular formula C10H9FO. It is a yellow liquid with a strong, sweet, and pungent odor, making it a valuable component in the production of fragrances and flavors. Its aromatic and unsaturated structure also renders it a versatile reactant in organic synthesis, contributing to the creation of a wide array of compounds and materials. Furthermore, 4-Fluorocinnamaldehyde finds application in the pharmaceutical industry, where it is utilized for the synthesis of specific pharmaceutical compounds and in research applications.
Uses
Used in Fragrance and Flavor Industry:
1-(4-fluorophenyl)buta-2,3-dien-1-one is used as a key component in the production of fragrances and flavors due to its strong, sweet, and pungent odor. Its distinctive scent profile makes it a popular choice for enhancing the sensory appeal of various consumer products.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-fluorophenyl)buta-2,3-dien-1-one is used as a versatile reactant. Its aromatic and unsaturated structure allows for a wide range of chemical reactions, enabling the production of diverse compounds and materials.
Used in Pharmaceutical Industry:
1-(4-fluorophenyl)buta-2,3-dien-1-one is employed in the pharmaceutical industry for the synthesis of certain pharmaceutical compounds. Its unique chemical properties make it a valuable asset in the development of new drugs and therapeutic agents.
Used in Research Applications:
In addition to its practical applications, 1-(4-fluorophenyl)buta-2,3-dien-1-one is also utilized in research settings. Its distinctive chemical structure and properties make it an interesting subject for scientific inquiry, potentially leading to new discoveries and advancements in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1223611-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,6,1 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1223611-91:
(9*1)+(8*2)+(7*2)+(6*3)+(5*6)+(4*1)+(3*1)+(2*9)+(1*1)=113
113 % 10 = 3
So 1223611-91-3 is a valid CAS Registry Number.
1223611-91-3Relevant articles and documents
Synthesis of vinylic sulfones in aqueous media
Goh, Jeffrey,Maraswami, Manikantha,Loh, Teck-Peng
, p. 1060 - 1065 (2021/02/16)
A green method for the sulfination of allenic carbonyl compounds to access a wide variety of vinylic sulfones is developed. This reaction works in aqueous media under very mild conditions. This reaction is atom economic. A wide variety of vinylic sulfones could be obtained in moderate to excellent yields with wide functional group tolerance. The efficiency of this method is demonstrated in some reactions where the desired products can be isolated by filtration.
Revisiting the Addition of in-situ Nucleophiles to Allenic Ketones: An Entry Towards Synthesis of Benzodioxins
Sahoo, Sushree Ranjan,Sarkar, Debayan
, p. 1727 - 1731 (2020/03/13)
The manuscript delineates a revisit towards regioselective addition of in situ generated negative nucleophiles to allenic ketones in the presence of a base. A wide variety of allenic ketones as well as nucleophiles are viable in this transformation. A dir
Synthesis of 1,2-allenic ketones through oxidation of homopropargyl alcohols with CrO3(cat.)/TBHP under MWI
Zhang, Xin Ying,Qu, Ying Ying,Wang, Yang Yang,Fan, Xue Sen
experimental part, p. 268 - 271 (2012/01/30)
A CrO3 catalyzed oxidation of homopropargyl alcohols with tert-butyl hydroperoxide under microwave irradiation was found to be an efficient and rapid alternative for the preparation of 1,2-allenic ketones. The advantages of this procedure inclu
