56952-04-6 Usage
Uses
Used in Chemical Reactions:
Methyl (Z)-2-Benzoylamino-3-Dimethylaminopropenoate is used as a reactant in various chemical reactions for its ability to act as both a donor and acceptor of hydrogen bonds, facilitating the formation of new compounds and products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl (Z)-2-Benzoylamino-3-Dimethylaminopropenoate is used as a potential building block for the synthesis of new drug molecules, given its unique structure and functional groups that can be manipulated in chemical reactions to create novel therapeutic agents.
Used in Material Science:
Methyl (Z)-2-Benzoylamino-3-Dimethylaminopropenoate is used as a component in the development of new materials, such as polymers and composites, due to its potential to form stable bonds and contribute to the overall properties of the material.
Used in Research and Development:
In research and development settings, Methyl (Z)-2-Benzoylamino-3-Dimethylaminopropenoate is used as a subject of study to explore its chemical properties, reactivity, and potential applications in various fields, including but not limited to chemistry, materials science, and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 56952-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,5 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56952-04:
(7*5)+(6*6)+(5*9)+(4*5)+(3*2)+(2*0)+(1*4)=146
146 % 10 = 6
So 56952-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2O3/c1-15(2)9-11(13(17)18-3)14-12(16)10-7-5-4-6-8-10/h4-9H,1-3H3,(H,14,16)
56952-04-6Relevant academic research and scientific papers
Highly enantioselective synthesis of α,β-diaminopropanoic acid derivatives using a catalytic asymmetric hydrogenation approach
Robinson,Chin Yu Lim,He,Ma,Li
, p. 4141 - 4147 (2007/10/03)
Rh-DuPhos-catalyzed asymmetric hydrogenation of α,β-diamidoacrylates provides a highly efficient and enantioselective route to chiral α,β-diaminopropanoic acid derivatives. The mechanistic course of the hydrogenation was studied using isotopically enriched enamide complexes and phosphorus and carbon NMR. Addition of methyl α-N-benzoyl-β-N-acetyl-diaminopropenoate to the solvated catalyst gave a single 1:1 enamide complex and demonstrated the binding of the olefin and α-amide carbonyl group; the carboxylate and β-N-acyl groups did not bind to the metal. Changes to the electronic and steric properties of the β-N-acyl group were well tolerated; however, small changes to the binding α-N-acyl group were found to significantly affect hydrogenation yields.
TRANSFORMATION OF AMINES AND N-HETEROARYLFORMAMIDINES INTO ESTERS OF SUBSTITUTED β-AMINO-α,β-DEHYDRO-α-AMINO ACIDS
Stanovnik, Branko,Svete, Jurij,Tisler, Miha,Zorz, Lilijana,Hvala, Ales,Simonic, Igor
, p. 903 - 910 (2007/10/02)
Esters of substituted β-amino-α,β-dehydro-α-amino acids 5 were prepared either by transformation of N-heteroaryl-N,N-dimethylformamidines 2 with 3 into 4, followed by ring opening, or by treatment of primary or secondary amines 1 with 9.
