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2-phenyl-5,5-bis<(benzyloxy)methyl>-1,3-dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82265-10-9

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82265-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82265-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82265-10:
(7*8)+(6*2)+(5*2)+(4*6)+(3*5)+(2*1)+(1*0)=119
119 % 10 = 9
So 82265-10-9 is a valid CAS Registry Number.

82265-10-9Relevant academic research and scientific papers

Synthesis of new cores and their use in the preparation of polyester dendrimers

Twibanire, Jean-D'Amour K.,Al-Mughaid, Hussein,Grindley, T. Bruce

experimental part, p. 9602 - 9609 (2011/01/03)

Six dendrimer and dendron cores terminated by hydroxyl groups that are neither phenolic nor cleavable by hydrogenolysis have been prepared in a consistent one-pot manner from terminal allyl groups by reduction of the product of reductive ozonolysis. Some of the terminal allyl derivatives are new and others have been prepared by new methods. The well-known O-benzylidene derivative of 2,2′-bis(hydroxymethyl)propanoic acid was shown to be the cis-stereoisomer. A new AB3-type anhydride, tris(benzyloxymethyl) acetic anhydride has been prepared. It was demonstrated that these cores and dendrons could be assembled into first and second generation homo- and mixed polyester dendrimers.

Synthesis of achiral α,α-disubstituted β-alanines, and their use in construction of libraries of β-peptide conjugates of N-2-alkyl-1,2,3,4- tetrahydroisoquinolines on a solid support

Heinonen, Petri,Virta, Pasi,Loennberg, Harri

, p. 7613 - 7624 (2007/10/03)

Six achiral N-phthaloyl protected α,α-disubstituted β-amino acids were synthesized, and used to construct a 96 compound library of 1,2,3,4- tetrahydroisoquinoline conjugates of β-peptides on a solid support. The library synthesis consisted of attachment of an appropriately 5-O-tethered 1,2,3,4-tetrahydroisoquinoline via the N-2 atom to a vinyl sulfonyl support, elongation of the deprotected 5-O-tether by repeated peptide coupling, quaternarization of N-2 with alkylamines and release of the β-peptide conjugate into solution with triethylamine.

Polytopic Cation Receptors. 2. Synthesis and Selective Complex Formation of Spiro-Linked "Multiloop Crown Compounds"

Weber, Edwin

, p. 3478 - 3486 (2007/10/02)

A new type of crown compound (1-10) featuring a spiro-linked assembly of two to four individual macrorings differing in ring size, rigidity, and donor characteristics is synthesized.Syntheses were achieved by means of high-dilution techniques and blocking/deblocking procedures beginning with pentaerythritol as the basic building block.The ability of the new ligands ("multiloop crown compounds") to selectively form crystalline polyhomonuclear/heteronuclear complexes is studied.It is found that the symmetrically looped molecules (1a-c, 4a, 6, 7d) can incorporate two orthree identical metal cations well matched in their diameter (Li+, Na+, K+, Ca2+, Ba2+).Cations which are too large to fit into the crown rings of 1a-c complex in a sandwich-like manner; those which are too small effect a high hydration in their complexes.Asymmetrical 1d and 9 allow the common uptake of different metal ions, e.g., a combination of Li+ and Ba2+ or of 2K+ and Co2+.The specific occupation of the different subrings is discussed.Ligand 1b is shown to discriminate Ca2+ from Na+; 1c and 6 preferentially complex Ba2+ from a Ba2+/K+ mixture.Thus, the new ligands act as manifold selective cation receptors, corresponding to the specification of their binding compartments.

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