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869116-46-1

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869116-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869116-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,1,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 869116-46:
(8*8)+(7*6)+(6*9)+(5*1)+(4*1)+(3*6)+(2*4)+(1*6)=201
201 % 10 = 1
So 869116-46-1 is a valid CAS Registry Number.

869116-46-1Relevant articles and documents

Synthesis and characterization of some novel copper(II) complexes with an optically active Betti base

Bhatt, Shardul,Trivedi, Bhavna

scheme or table, p. 15 - 22 (2012/05/20)

Novel Cu(II) complexes with racemic as well as optically pure 1-(α-amino benzyl)-2-napthol, commonly known as Betti base, and its derivative 1-(α-pyrrolidinyl benzyl)-2-napthol have been synthesized. The general composition of all the isolated complexes, as determined by elemental analysis, thermal analysis and FAB mass spectra, is found to be Cu(L-H) 2. The coordination of the ligand with metal has been confirmed by IR and ESR spectra of the complexes. The CD spectra of complexes with the S-form of the ligands exhibit a mirror image relationship with the CD spectra of the complexes with the corresponding R-form of the ligands. The Cu(II) complex with racemic Betti base has been characterized structurally. It crystallizes in the monoclinic space group P21/c. The complexes display quasi reversible redox behavior due to the Cu(II)/Cu(I) reduction process.

An efficient kinetic resolution of racemic betti base based on an enantioselective N,O-deketalization

Dong, Yanmei,Li, Rui,Lu, Jun,Xu, Xuenong,Wang, Xinyan,Hu, Yuefei

, p. 8617 - 8620 (2007/10/03)

An efficient kinetic resolution of racemic Betti base with L-(+)-tartaric acid in acetone was developed based on a novel enantioselective N,O-deketalization, by which the enantiopure R- and S-enantiomers of Betti base were obtained as the corresponding N,

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