100393-41-7 Usage
General Description
3-Amino-3-Naphthalen-1-yl-Propionic Acid is a chemical compound that belongs to the class of organic compounds known as naphthalenecarboxylic acids and derivatives, which are compounds containing a naphthalene moiety (a polycyclic aromatic hydrocarbon made up of two fused benzene rings) which bears a carboxylic acid group or a derivative thereof. These compounds are characterized by a naphthalene ring structure attached to a propionic acid group with an amino group. They are used in a variety of chemical and biochemical research due to their unique properties. The properties of these compounds can be altered based on what they are complexed with, leading to diverse applications. However, the specifics of this compound's usage or any potential health effects are not widely available, thus additional research is required to fully understand this compound's utility and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 100393-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,9 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100393-41:
(8*1)+(7*0)+(6*0)+(5*3)+(4*9)+(3*3)+(2*4)+(1*1)=77
77 % 10 = 7
So 100393-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c14-12(8-13(15)16)11-7-3-5-9-4-1-2-6-10(9)11/h1-7,12H,8,14H2,(H,15,16)/t12-/m1/s1
100393-41-7Relevant articles and documents
Ruthenium-catalyzed asymmetric epoxidation of olefins using H 2O2, part I: Synthesis of new chiral N,N,N,-tridentate pybox and pyboxazine ligands and their ruthenium complexes
Tse, Man Kin,Bhor, Santosh,Klawonn, Markus,Anilkumar, Gopinathan,Jiao, Haijun,Doebler, Christian,Spannenberg, Anke,Magerlein, Wolfgang,Hugl, Herbert,Beller, Matthias
, p. 1855 - 1874 (2008/02/02)
The synthesis of chiral tridentate N,N,N-pyridine-2.6-bisoxazolines 3 (pyhox ligands) and N,N,N-pyridine-2.6-bisoxazines 4 (pyboxazine ligands) is described in detail. These novel ligands constitute a useful tool-box for the application in asymmetric catalysis. Compounds 3 and 4 are conveniently prepared by cyclization of enantiomerically pure α- or β-amino al cohols with dimethyl pyridine-2,6-dicarboximidate. The corresponding ruthenium complexes are efficient asymmetric epoxidation catalysts and have been prepared in good yield and fully char acterized by spectroscopic means. Four of these ruthenium complexes have been characterized by X-ray crystallography. For the first time the molecular structure of a pyboxazine complex (2,6-bis-[(4S)-4-phenyl-5,6- dihydro-4H-[1,3]oxazinyl]pyridine)(pyridine-2,6-dicarboxylate)ruthenium (S)-2aa, is presented.
