507472-11-9 Usage
Uses
Used in Pharmaceutical Research:
FMOC-(S)-3-AMINO-3-(2-NAPHTHYL)-PROPIONIC ACID is used as a building block in the synthesis of chiral peptides and drugs, leveraging its enantiomeric properties for the development of new pharmaceuticals with specific biological activities.
Used in Peptide Synthesis:
In the field of peptide synthesis, FMOC-(S)-3-AMINO-3-(2-NAPHTHYL)-PROPIONIC ACID is used as a key component for constructing complex peptide sequences, taking advantage of its FMOC group for easy detection and purification during the synthesis process.
Used in Chemical Research:
FMOC-(S)-3-AMINO-3-(2-NAPHTHYL)-PROPIONIC ACID is utilized as a research tool in chemical studies, particularly for investigating the properties and interactions of chiral compounds and their potential applications in various chemical processes.
Used in Biomaterial Development:
In the development of biomaterials, FMOC-(S)-3-AMINO-3-(2-NAPHTHYL)-PROPIONIC ACID is employed as a component in the synthesis of materials with specific biological properties, such as chiral recognition or fluorescence, which can be applied in areas like drug delivery or tissue engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 507472-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,4,7 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 507472-11:
(8*5)+(7*0)+(6*7)+(5*4)+(4*7)+(3*2)+(2*1)+(1*1)=139
139 % 10 = 9
So 507472-11-9 is a valid CAS Registry Number.
507472-11-9Relevant academic research and scientific papers
Gandhi, Shikha,List, Benjamin
, p. 2573 - 2576 (2013)
It takes three to make things go right: The first direct asymmetric three-component reaction of aldehydes, carbamates, and allyltrimethylsilane leading to enantioenriched homoallylic amines has been developed using a new chiral disulfonimide catalyst (see scheme). The method employs readily available, inexpensive, and nontoxic starting materials and is applicable to both aromatic and aliphatic aldehydes. Copyright
