58997-90-3 Usage
General Description
The chemical "2-(dimethylamino)-2-phenylbutyl (-)-3,4,5-trimethoxybenzoate" is a compound that belongs to the class of organic compounds known as benzoic acid esters. It is a synthetic compound that contains a benzoate ester linked to a 2-(dimethylamino)-2-phenylbutyl group. The compound also contains three methoxy groups attached to the benzene ring. This chemical compound has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications. It may have physiological effects on the central nervous system due to the presence of the dimethylamino group, and the trimethoxybenzoate structure may also exhibit biological activity. Further research and testing are needed to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 58997-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58997-90:
(7*5)+(6*8)+(5*9)+(4*9)+(3*7)+(2*9)+(1*0)=203
203 % 10 = 3
So 58997-90-3 is a valid CAS Registry Number.
58997-90-3Relevant articles and documents
Direct Conversion of N-Alkylamines to N-Propargylamines through C-H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage Functionalization of Bioactive Molecules
Chan, Jessica Z.,Yesilcimen, Ahmet,Cao, Min,Zhang, Yuyang,Zhang, Bochao,Wasa, Masayuki
supporting information, p. 16493 - 16505 (2020/10/26)
An efficient catalytic method to convert an α-C-H bond of N-alkylamines into an α-C-alkynyl bond was developed. In the past, such transformations were carried out under oxidative conditions, and the enantioselective variants were confined to tetrahydroisoquinoline derivatives. Here, we disclose a method for the union of N-alkylamines and trimethylsilyl alkynes, without the presence of an external oxidant and promoted through cooperative actions of two Lewis acids, B(C6F5)3 and a Cu-based complex. A variety of propargylamines can be synthesized in high diastereo-and enantioselectivity. The utility of the approach is demonstrated by the late-stage site-selective modification of bioactive amines. Kinetic investigations that shed light on various mechanistic nuances of the catalytic process are presented.
