5747-06-8 Usage
Description
4-Phenyl-4-Pentenoic Acid is a chemical compound with the molecular formula C11H12O2. It is an unsaturated carboxylic acid featuring a phenyl group (C6H5) attached to the fourth carbon of a pentenoic acid chain. This unique structure and reactivity make it a valuable component in various chemical processes and applications.
Uses
Used in Organic Synthesis:
4-Phenyl-4-Pentenoic Acid is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for versatile reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Phenyl-4-Pentenoic Acid is used as a building block for the development of new drugs. Its potential biological activities have been studied, and it is considered a promising candidate for the treatment of various diseases.
Used as a Flavoring Agent:
4-Phenyl-4-Pentenoic Acid is used as a flavoring agent in the food and beverage industry. Its unique chemical structure contributes to the development of distinct flavors and scents, enhancing the sensory experience of various products.
Used in Polymer Synthesis:
In the polymer industry, 4-Phenyl-4-Pentenoic Acid is utilized in the synthesis of polymers with specific properties. Its incorporation into polymer chains can lead to materials with tailored characteristics, such as improved strength, flexibility, or thermal stability.
Used as a Precursor in Compound Production:
4-Phenyl-4-Pentenoic Acid serves as a precursor in the production of various compounds, including specialty chemicals and materials. Its reactivity and structural features make it an essential component in the synthesis of these advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5747-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5747-06:
(6*5)+(5*7)+(4*4)+(3*7)+(2*0)+(1*6)=108
108 % 10 = 8
So 5747-06-8 is a valid CAS Registry Number.
5747-06-8Relevant articles and documents
Are bis(pyridine)iodine(i) complexes applicable for asymmetric halogenation?
Andreasson, M?ns,Erdelyi, Mate,Németh, Flóra Boróka,Pápai, Imre,Sethio, Daniel,von der Heiden, Daniel
supporting information, p. 8307 - 8323 (2021/10/12)
Enantiopure halogenated molecules are of tremendous importance as synthetic intermediates in the construction of pharmaceuticals, fragrances, flavours, natural products, pesticides, and functional materials. Enantioselective halofunctionalizations remain
Development of Nitrolactonization Mediated by Iron(III) Nitrate Nonahydrate
Yoshimura, Tomoyuki,Umeda, Yuki,Takahashi, Risako,Matsuo, Jun-Ichi
, p. 1220 - 1225 (2020/12/17)
The nitrolactonization of alkenyl carboxylic acids mediated by Fe(NO3)3·9H2O has been developed. Nitrolactones were obtained in up to 93% yield by treatment of alkenyl carboxylic acids with Fe(NO3)3·9H2O. Mechanistic studies disclosed that the reaction proceeded through a radical intermediate generated from addition of NO2 to alkenyl carboxylic acids.
Copper-Catalyzed Modular Amino Oxygenation of Alkenes: Access to Diverse 1,2-Amino Oxygen-Containing Skeletons
Hemric, Brett N.,Chen, Andy W.,Wang, Qiu
supporting information, p. 1468 - 1488 (2019/01/25)
Copper-catalyzed alkene amino oxygenation reactions using O-acylhydroxylamines have been achieved for a rapid and modular access to diverse 1,2-amino oxygen-containing molecules. This transformation is applicable to the use of alcohols, carbonyls, oximes, and thio-carboxylic acids as nucleophiles on both terminal and internal alkenes. Mild reaction conditions tolerate a wide range of functional groups, including ether, ester, amide, carbamate, and halide. The reaction protocol allows for starting with free amines as the precursor of O-benzoylhydroxylamines to eliminate their isolation and purification, contributing to broader synthetic utilities. Mechanistic investigations reveal the amino oxygenation reactions may involve distinct pathways, depending on different oxygen nucleophiles.
