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1,3,5,7-tetrakis(hydroxymethyl)adamantane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75534-58-6

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75534-58-6 Usage

Class

Adamantane derivatives

Structure

Cage-like molecule with four hydroxymethyl groups attached to carbon atoms at positions 1, 3, 5, and 7

Thermal stability

High

Applications

a. Building block for functionalized nanostructured materials
b. Polymer composites
c. Nanocomposites
d. Advanced ceramics
e. Drug delivery
f. Catalysis
g. Surface modification

Potential uses

Energy storage (enhancing performance of lithium-ion batteries and fuel cells)

Check Digit Verification of cas no

The CAS Registry Mumber 75534-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,3 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75534-58:
(7*7)+(6*5)+(5*5)+(4*3)+(3*4)+(2*5)+(1*8)=146
146 % 10 = 6
So 75534-58-6 is a valid CAS Registry Number.

75534-58-6Relevant academic research and scientific papers

Four-Directional synthesis of adamantane derivatives

Qu, Tao,White, Andrew J. P.,Barrett, Anthony G. M.

, p. 18 - 50 (2020/08/28)

1-Adamantanemethanol, 1,3-adamantanedimethanol and 1,3,5,7-adamantanetetramethanol were converted into adamantanes functionalized with one or four (2R,1S)-2-formyl-1-cyclopropyl residues using Charette enantioselective cyclopropanation reactions and with one, two or four 4-ethoxy- (or 4-t-butoxy)-3-diazo-2,4- dioxobutyl residues from aldehyde and diazo-acetate ester condensation reactions by 1-directional, 2- directional or 4-directional syntheses. The synthesis of adamantane fused to cyclopentadiene is also reported. 'Equation Presented'.

Non-Interpenetrated Single-Crystal Covalent Organic Frameworks

Han, Jing,Liang, Lin,Luo, Yi,Ma, Tianqiong,Ni, Jianwei,Niu, Jing,Qiu, Yi,Sun, Junliang,Wang, Wei,Wang, Wei David,Wang, Zhi-Peng,Yin, Guan-Lin,Yu, Wei,Zhang, Lei

supporting information, p. 17991 - 17995 (2020/08/19)

Growth of covalent organic frameworks (COFs) as single crystals is extremely challenging. Inaccessibility of open-structured single-crystal COFs prevents the exploration of structure-oriented applications. Herein we report for the first time a non-interpenetrated single-crystal COF, LZU-306, which possesses the open structure constructed exclusively via covalent assembly. With a high void volume of 80 %, LZU-306 was applied to investigate the intrinsic dynamics of reticulated tetraphenylethylene (TPE) as the individual aggregation-induced-emission moiety. Solid-state 2H NMR investigation has determined that the rotation of benzene rings in TPE, being the freest among the reported cases, is as fast as 1.0×104 Hz at 203 K to 1.5×107 Hz at 293 K. This research not only explores a new paradigm for single-crystal growth of open frameworks, but also provides a unique matrix-isolation platform to reticulate functional moieties into a well-defined and isolated state.

Chromophore Multiplication To Enable Exciton Delocalization and Triplet Diffusion Following Singlet Fission in Tetrameric Pentacene

Hetzer, Constantin,Basel, Bettina S.,Kopp, Sebastian M.,Hampel, Frank,White, Fraser J.,Clark, Timothy,Guldi, Dirk M.,Tykwinski, Rik R.

supporting information, p. 15263 - 15267 (2019/10/22)

A tetrameric pentacene, PT, has been used to explore the effects of exciton delocalization on singlet fission (SF). For the first time, triplet decorrelation through intramolecular triplet diffusion was observed following SF. Transient absorption spectros

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