62240-37-3 Usage
Description
2-(Aminoethyl)-2-methyl-1,3-dioxolane is an organic compound characterized by its unique structure, which features a dioxolane ring with an aminoethyl and a methyl group attached to the second carbon. 2-(Aminoethyl)-2-methyl-1,3-dioxolane is known for its potential applications in various fields due to its chemical properties.
Uses
Used in Pharmaceutical Industry:
2-(Aminoethyl)-2-methyl-1,3-dioxolane is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
2-(Aminoethyl)-2-methyl-1,3-dioxolane is used as a building block in the total synthesis of complex organic molecules, such as (+/-)-Methyl Homodaphniphyllate, for its ability to be modified and functionalized to create diverse chemical entities with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62240-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62240-37:
(7*6)+(6*2)+(5*2)+(4*4)+(3*0)+(2*3)+(1*7)=93
93 % 10 = 3
So 62240-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-6(2-3-7)8-4-5-9-6/h2-5,7H2,1H3
62240-37-3Relevant articles and documents
Highly Regioselective 5-endo-tet Cyclization of 3,4-Epoxy Amines into 3-Hydroxypyrrolidines Catalyzed by La(OTf)3
Hoshino, Yoshihiko,Iwabuchi, Yoshiharu,Kuriyama, Yuse,Sasano, Yusuke,Uesugi, Shun-ichiro,Yamaichi, Aoto
supporting information, p. 1961 - 1965 (2021/01/04)
Highly regioselective intramolecular aminolysis of 3,4-epoxy amines has been achieved. Key features of this reaction are (1) chemoselective activation of epoxides in the presence of unprotected aliphatic amines in the same molecules by a La(OTf)3 catalyst and (2) excellent regioselectivity for anti-Baldwin 5-endo-tet cyclization. This reaction affords 3-hydroxy-2-alkylpyrrolidines stereospecifically in high yields. DFT calculations revealed that the regioselectivity might be attributed to distortion energies of epoxy amine substrates. The use of this reaction was demonstrated by the first enantioselective synthesis of an antispasmodic agent prifinium bromide.
New efficient synthesis of pyrido[2,3-c] and pyrido[3,2-c]coumarin derivatives
Pavé, Grégoire,Chalard, Pierre,Viaud-Massuard, Marie-Claude,Troin, Yves,Guillaumet, Gérald
, p. 987 - 990 (2007/10/03)
Various substituted pyrido[2,3-c] and pyrido[3,2-c]coumarins are efficiently prepared in three steps from 3- and 4-hydroxycoumarins, respectively and protected β-aminoketones.
