6797-70-2 Usage
Description
α-(DiethylaMino)benzeneacetic Acid Ethyl Ester, also known as an amino ester reagent, is a chemical compound derived from the esterification of α-(diethylamino)benzeneacetic acid with ethanol. It possesses a unique chemical structure that allows it to participate in various chemical reactions and has potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
α-(DiethylaMino)benzeneacetic Acid Ethyl Ester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its ability to form α-aminoaldehydes makes it a valuable reagent in the preparation of complex organic molecules, which can be further utilized in the development of new drugs and therapeutic agents.
Used in Chemical Research:
In the field of chemical research, α-(DiethylaMino)benzeneacetic Acid Ethyl Ester serves as a versatile reagent for the synthesis of various organic compounds. Its unique chemical properties enable researchers to explore new reaction pathways and develop innovative synthetic methods, contributing to the advancement of chemical science.
Used in Organic Synthesis:
α-(DiethylaMino)benzeneacetic Acid Ethyl Ester is used as a key building block in organic synthesis, particularly for the preparation of α-aminoaldehydes. These α-aminoaldehydes can be further transformed into a wide range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals, making it an essential component in the synthesis of various industrial products.
Check Digit Verification of cas no
The CAS Registry Mumber 6797-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6797-70:
(6*6)+(5*7)+(4*9)+(3*7)+(2*7)+(1*0)=142
142 % 10 = 2
So 6797-70-2 is a valid CAS Registry Number.
6797-70-2Relevant articles and documents
Umpolung Reactions of α-Tosyloximino Esters in a Flow System
Ota, Kazuki,Fukumoto, Shinya,Iwase, Taiki,Mizota, Isao,Shimizu, Makoto,Hachiya, Iwao
supporting information, p. 1930 - 1936 (2020/09/18)
An umpolung reaction of α-tosyloximino esters in a flow system is disclosed. Tandem N, N-dialkylations with two different Grignard reagents gave the desired N, N-dialkylated products in moderate to good yields. In addition, a tandem N, N, C-trialkylation of an α-tosyloximino ester with three different Grignard reagents has been successfully achieved to afford the desired N, N, C-trialkylated product in moderate yield.
N,N-Di- and N,N,C-Trialkylation of δ-sulfoximino esters
Hata, Shingo,Maeda, Tatsuya,Shimizu, Makoto
, p. 1203 - 1205 (2013/01/15)
N,N-Dialkylation of α-sulfoximino esters with Grignard reagents proceeds to give α-N,N-dialkylamino esters. N,N,CTrialkylated product is also obtained via the oxidation and nucleophilic addition reaction of the intermediary enolate.
The Chemistry of N-Substituted Benzotriazoles Part 23. Synthesis of Tertiary α-Amino Esters
Katritzky, Alan R.,Urogdi, Laszlo,Mayence, Annie
, p. 323 - 327 (2007/10/02)
2-Dialkylaminoalkanoic esters 6 are prepared in good yield by the reaction of organozinc derivatives 5 with dialkylamino(1-benzotriazolyl)acetic esters 4, obtained from the condensation of secondary amines 3 with ethyl glyoxylate 2 and benzotriazole 1.
