56952-04-6 Usage
General Description
Methyl (Z)-2-Benzoylamino-3-dimethylaminopropenoate is a complex organic compound that belongs to the group of benzoic acids and derivatives. Its structure includes a benzoyl group, which indicates that it originates from benzoic acid. The compound also contains a dimethylamino group and a methyl ester. While there isn't a wealth of specific information available about this particular compound, the presence of these groups implies it may be used in various chemical reactions, particularly as it can act as both a donor and acceptor of hydrogen bonds. However, without more specific information, it is not possible to definitively state the applications and properties of Methyl (Z)-2-Benzoylamino-3-Dimethylaminopropenoate.
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 articles and documents
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.
