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886761-14-4

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886761-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 886761-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,7,6 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 886761-14:
(8*8)+(7*8)+(6*6)+(5*7)+(4*6)+(3*1)+(2*1)+(1*4)=224
224 % 10 = 4
So 886761-14-4 is a valid CAS Registry Number.

886761-14-4Relevant articles and documents

Self-assembly of dendritic crowns into chiral supramolecular spheres

Percec, Virgil,Imam, Mohammad R.,Peterca, Mihai,Wilson, Daniela A.,Heiney, Paul A.

supporting information; experimental part, p. 1294 - 1304 (2009/06/28)

The synthesis and structural and retrostructural analysis of a library of dendronized cyclotriv- eratrylene containing seven nonchiral and sevenchiral self-assembling dendrons is reported. These dendronized cyclotri veratrylenes exhibit a crown conformation that we named dendritic crown.Selected examples of dendritic crowns self-assemble into helical pyrami dal columns that self-organize into columnar crystals or into 2-D columnar hexagonal lattices with intracolumnar order. A second group of dendritic crowns self-assembles into helical pyramidal columns and spherical supramolecular dendrimers that self- organize into cubic and tetragonal lattices. A third group of dendritic crowns self-assembles only in spherical supramolecular dendrimers. The helical pyramidal columns and spherical supramolecular dendrimers assembled from dendronized cyclotriveratrylene containing nonchiral dendrons are chiral but racemic while those generated from chiral dendrons exhibit amplified chirality. Structural analysis by a combination of X-ray diffraction methods and CD experiments demonstrated a new mechanism for the assembly of chiral supramolecular spheres that involves an intramolecular structure containing short fragments of helical pyramidal columns.

Molecular structure of helical supramolecular dendrimers

Peterca, Mihai,Percec, Virgil,Imam, Mohammad R.,Leowanawat, Pawaret,Morimitsu, Kentaro,Heiney, Paul A.

supporting information; body text, p. 14840 - 14852 (2009/02/08)

The molecular structure of helical supramolecular dendrimers generated from self-assembling dendrons and dendrimers and from self-organizable dendronized polymers was elucidated for the first time by the simulation of the X-ray diffraction patterns of their oriented fibers. These simulations were based on helical diffraction theory applied to simplified atomic helical models, followed by Cerius2 calculations based on their complete molecular helical structures. Hundreds of samples were screened until a library containing 14 supramolecular dendrimers and dendronized polymers provided a sufficient number of helical features in the X-ray diffraction pattern of their oriented fibers. This combination of techniques provided examples of single-92 and -11 3 helices, triple-61, -81, -91, and -121 helices, and an octa-321 helix that were assembled from crownlike dendrimers, hollow and nonhollow supramolecular crownlike dendrimers, hollow and nonhollow supramolecular disklike dendrimers, and hollow and nonhollow supramolecular and macromolecular helicene-like architectures. The method elaborated here for the determination of the molecular helix structure was transplanted from the field of structural biology and will be applicable to other classes of synthetic helical assemblies. The determination of the molecular structure of helical supramolecular assemblies is expected to provide an additional level of precision in the design of helical functional assemblies resembling those from biological systems.

Propeller-like hydrogen-bonded banana-melamine complexes inducing helical supramolecular organizations

Barbera, Joaquin,Puig, Laura,Romero, Pilar,Serrano, Jose Luis,Sierra, Teresa

, p. 4487 - 4492 (2007/10/03)

The results of the study presented here show a new example of the use of liquid crystals and the interactions involved in the mesomorphic state to build up complex molecular organizations. We have pursued a design strategy in which hydrogen bonding allows

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