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52773-84-9

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52773-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52773-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,7 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52773-84:
(7*5)+(6*2)+(5*7)+(4*7)+(3*3)+(2*8)+(1*4)=139
139 % 10 = 9
So 52773-84-9 is a valid CAS Registry Number.

52773-84-9Relevant academic research and scientific papers

Exploring the scope of an α/β-aminomutase for the amination of cinnamate epoxides to arylserines and arylisoserines

Shee, Prakash K.,Ratnayake, Nishanka Dilini,Walter, Tyler,Goethe, Olivia,Onyeozili, Edith Ndubuaku,Walker, Kevin D.

, p. 7418 - 7430 (2019/08/20)

Biocatalytic process-development continues to advance toward discovering alternative transformation reactions to synthesize fine chemicals. Here, a 5-methylidene-3,5-dihydro-4H-imidazol-4-one (MIO)-dependent phenylalanine aminomutase from Taxus canadensis (TcPAM) was repurposed to irreversibly biocatalyze an intermolecular amine transfer reaction that converted ring-substituted trans-cinnamate epoxide racemates to their corresponding arylserines. From among 12 substrates, the aminomutase ring-opened 3′-Cl-cinnamate epoxide to 3′-Cl-phenylserine 140 times faster than it opened the 4′-Cl-isomer, which was turned over slowest among all epoxides tested. GC/MS analysis of chiral auxiliary derivatives of the biocatalyzed phenylserine analogues showed that the TcPAM-transamination reaction opened the epoxides enantio- A nd diastereoselectively. Each product mixture contained (2S)+(2R)-anti (erythro) and (2S)+(2R)-syn (threo) pairs with the anti-isomers predominating (-90:10 dr). Integrating the vicinal proton signals in the 1H NMR spectrum of the enzyme-catalyzed phenylserines and calculating the chemical shift difference (?"?) between the anti and syn proton signals confirmed the diastereomeric ratios and relative stereochemistries. Application of a (2S)-threonine aldolase from E. coli further established the absolute stereochemistry of the chiral derivatives of the diastereomeric enzymatically derived products. The 2R:2S ratio for the biocatalyzed anti-isomers was highest (88:12) for 3′-NO2-phenylserine and lowest (66:34) for 4′-F-phenylserine. This showed that the stereospecificity of TcPAM is in part directed by the substituent-type on the cinnamate epoxide analogue. The catalyst also converted each cinnamate epoxide analogue to its corresponding isoserine, highlighting a biocatalytic route to arylisoserines, which play a key role in building the pharmacophore seen in anticancer and protease inhibitor drugs.

Kinetics of the Pyridoxal-Catalyzed Dealdolation and β Elimination of Some Aromatic β-Hydroxy α-Amino Acids

Marcello, Joseph,Martell, Arthur E.

, p. 3441 - 3447 (2007/10/02)

The rates of dealdolation and β elimination of a number of para-substituted phenylserines have been determined by proton NMR.Electron-withdrawing substituents on the amino acid side chain enhance the dealdolation rate.In the substituted phenylserine β elimination and dealdolation were found to occur as parallel reactions.The metal ion-pyridoxal catalyzed systems undergo reaction more rapidly than the metal-free pyridoxal-catalyzed systems.A reaction mechanism for the parallel dealdolation and β-elimination reactions is proposed.In the case of one of the amino acids, phenylthreonine, the rate constants for the metal-free Schiff base were resolved into the specific rate constants for the individual solution components, and the variations obtained for the specific rate constants are interpreted in terms of the proposed reaction mechanism.

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