216690-15-2 Usage
Uses
Used in Pharmaceutical Industry:
Dimethyl 3-(4-fluorophenyl)glutarate is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs or treatments, potentially contributing to advancements in medicine.
Used as a Flavoring Agent:
In the food and beverage industry, dimethyl 3-(4-fluorophenyl)glutarate is employed as a flavoring agent. Its distinctive chemical properties enable it to impart specific tastes to food products, enhancing their flavor profiles.
Used as a Fragrance Ingredient:
The fragrance industry also leverages the properties of dimethyl 3-(4-fluorophenyl)glutarate, using it as an ingredient in the creation of various scents. Its aromatic characteristics can be used to develop unique fragrances for a range of applications, from perfumes to scented products.
Used as a Chemical Intermediate in Polymer and Plastics Production:
Dimethyl 3-(4-fluorophenyl)glutarate serves as a chemical intermediate in the production of polymers and plastics. Its role in the synthesis process is crucial for creating materials with specific properties, such as durability, flexibility, or heat resistance, which are essential for various industrial applications.
Potential Use in Medicine:
While not explicitly stated in the provided materials, the potential applications of dimethyl 3-(4-fluorophenyl)glutarate in the field of medicine could include its use in the development of new drugs or treatments, given its role as a building block in the synthesis of pharmaceuticals. Further research and development would be necessary to explore and validate these potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 216690-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,6,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 216690-15:
(8*2)+(7*1)+(6*6)+(5*6)+(4*9)+(3*0)+(2*1)+(1*5)=132
132 % 10 = 2
So 216690-15-2 is a valid CAS Registry Number.
216690-15-2Relevant academic research and scientific papers
Chemoselective hydrogenation of imides catalyzed by Cp*Ru(PN) complexes and its application to the asymmetric synthesis of paroxetine
Ito, Masato,Sakaguchi, Ayaka,Kobayashi, Chika,Ikariya, Takao
, p. 290 - 291 (2008/04/18)
This work represents the first catalytic hydrogenation of imides into amides and primary alcohols, in which the unique chemoselectivity is originated from the bifunctional nature of ruthenium-NH moiety in the catalyst. Copyright
Novel process
-
, (2008/06/13)
Compounds of structure (1) are obtained by reduction of compounds of the structures Compounds of structure (1), especially where Z is a hydrogen atom or a 3,4-methylenedioxyphenyl group, are important intermediates for inter alia paroxetine.
Asymmetric synthesis of (-)-paroxetine using PLE hydrolysis
Yu, Marvin S.,Lantos, Ivan,Peng, Zhi-Qiang,Yu,Cacchio, Thomas
, p. 5647 - 5651 (2007/10/03)
(-)-Paroxetine hydrochloride was produced asymmetrically in seven steps starting from 4-fluoro-benzaldehyde. The stereocenter at C-4 was initially set through desymmetrization of glutaric acid bis methyl ester 4 by PLE hydrolysis. A unique one-pot reduction-alkylation procedure was then developed to provide entry to lactam 2 with the appropriate absolute stereochemistry. (C) 2000 Elsevier Science Ltd.
