105-71-5 Usage
Description
Methyl N-(3-methoxy-3-oxopropyl)-N-methyl-beta-alaninate is a chemical compound that features a methyl group, a beta-alanine group, and a methoxy-oxopropyl group. methyl N-(3-methoxy-3-oxopropyl)-N-methyl-beta-alaninate is recognized for its potential pharmacological properties and is utilized in organic synthesis and pharmaceutical research. Its structure indicates possible biological activity, as it includes a beta-alanine derivative known for its association with reduced fatigue and enhanced exercise performance. Furthermore, the methoxy-oxopropyl group endows it with specific chemical reactivity, rendering it valuable in drug development and as a component for more intricate organic compounds.
Uses
Used in Pharmaceutical Research:
Methyl N-(3-methoxy-3-oxopropyl)-N-methyl-beta-alaninate serves as a key intermediate in pharmaceutical research for the development of new drugs. Its unique structure allows for the exploration of its potential therapeutic effects and incorporation into medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, methyl N-(3-methoxy-3-oxopropyl)-N-methyl-beta-alaninate is used as a building block for creating more complex organic compounds. Its methoxy-oxopropyl group provides specific reactivity that can be harnessed to form a variety of chemical products.
Used in Sports Nutrition:
Given its beta-alanine derivative component, which is linked to reduced fatigue and improved exercise performance, methyl N-(3-methoxy-3-oxopropyl)-N-methyl-beta-alaninate may also find applications in sports nutrition, potentially as an ingredient in supplements designed to enhance physical performance and endurance.
Check Digit Verification of cas no
The CAS Registry Mumber 105-71-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105-71:
(5*1)+(4*0)+(3*5)+(2*7)+(1*1)=35
35 % 10 = 5
So 105-71-5 is a valid CAS Registry Number.
105-71-5Relevant articles and documents
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Cook,Reed
, p. 399,401 (1945)
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ACRIDIN-9-YL-AMINE, QUINOLIN-9-YL-AMINE, 1 -AMINO-9H-THIOXANTHENE-9-ONE AND BENZO[B][1,5]NAPHTHYRI DIN-10-YL-AMINE DERIVATIVES AS AUTOPHAGY INHIBITORS FOR TREATING CANCER
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Paragraph 0307, (2021/07/17)
This disclosure provides a cridin-9-yl-amine, quinolin-9-yl-amine, 1- amino-9H-thioxanthene-9-one and benzo[b][l,5]naphthyridin-10- yl-amine derivatives and structurally related compounds for use as autophagy inhibitors for treating cancer. The present description discloses the synthesis and characterisation of exemplary compounds as well as pharmacological data thereof (e.g. pages 77 to 155; examples 1 to 22; compound A; compounds 1 to 21; tables 1 to 3).
Synthesis and structural characterization of zirconium complexes containing aminodiolate ligands and their use as Lewis acid catalysts
Shao, Pengcheng,Gendron, Roland A.L.,Berg, David J.
, p. 255 - 264 (2007/10/03)
A series of aminodiols RN(CH2CH2C(OH)R′2)2 (R, R′ = Me, Me 4; Me, Ph 5; tert-butyl, Me 6; tert-Bu, Ph 7; (S)-PhCH(Me), Me 8) were prepared by the Michael addition of a primary amine to methyl acrylate followed by reaction of the resulting aminodiester with excess methyl or phenyl lithium. Reaction of two equivalents of the aminodiols 4-8 with tetrabenzylzirconium afforded the zirconium bis(aminodiolates) 10-14 in excellent yield. Complex 11 (R, R′ = Me, Ph) adopts a cis, fac-octahedral geometry in solution and in the solid state. Complexes 10-14 are fluxional in solution by NMR spectroscopy: small substituents at nitrogen and large substituents at the alkoxide carbons slow the rate of exchange. The chiral complex 14 functions as a Lewis acid catalyst in the nitroaldol (Henry) reaction and the oxidation of geraniol by tert-butyl hydroperoxide with modest enantioselectivities (30 and 46% enantiomeric excess (ee), respectively).
