129042-60-0 Usage
General Description
3-Amino-3-benzo[1,3]dioxol-5-yl-propionic acid is a chemical compound with the molecular formula C11H11NO5. It contains a benzodioxole ring and an amine group, making it an important building block in organic chemistry. 3-Amino-3-benzo[1,3]dioxol-5-yl-propionic acid has potential applications in the pharmaceutical industry, as it can be used in the synthesis of various pharmaceutical drugs. Additionally, it has been studied for its biological properties and potential therapeutic uses. The compound is known for its potential antifungal and antibacterial properties, as well as its ability to inhibit certain enzymes. Overall, 3-Amino-3-benzo[1,3]dioxol-5-yl-propionic acid is a versatile chemical with potential applications in various fields, particularly in drug development and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 129042-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,4 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129042-60:
(8*1)+(7*2)+(6*9)+(5*0)+(4*4)+(3*2)+(2*6)+(1*0)=110
110 % 10 = 0
So 129042-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO4/c11-7(4-10(12)13)6-1-2-8-9(3-6)15-5-14-8/h1-3,7H,4-5,11H2,(H,12,13)
129042-60-0Relevant articles and documents
Kinetic resolution of aromatic β-amino acids by ω-transaminase
Bea, Han-Seop,Park, Hye-Jeong,Lee, Sang-Hyeup,Yun, Hyungdon
, p. 5894 - 5896 (2011)
Racemic aromatic β-amino acids have been kinetically resolved into (R)-β-amino acids with high enantiomeric excess (>99%) by a novel ω-TA with ca. 50% conversion.
An efficient new enzymatic method for the preparation of β-aryl-β-amino acid enantiomers
Tasnadi, Gabor,Forro, Eniko,Fueloep, Ferenc
, p. 2072 - 2077 (2008/12/22)
An efficient synthesis of β-aryl-β-amino acid enantiomers has been developed via the lipase-catalysed enantioselective hydrolysis of the corresponding racemic ethyl esters in an organic solvent. High enantioselectivities (E >100) were observed when the lipase PS-catalysed reactions were performed with H2O (0.5 equiv) in diisopropyl ether at 45 °C. The products could be easily separated and were obtained in good yields of ≥40%.
Heterocyclic anti-epileptogenic agents and methods of use thereof
-
, (2008/06/13)
Methods and compounds, such as β-heterocyclic-β-amino acids, useful for the inhibition of epileptogenesis are disclosed. Methods for preparing and using the β-heterocyclic-β-amino acids of the invention are also described.
