106510-41-2 Usage
Molecular structure
HCA is a long-chain unsaturated fatty acid with 27 carbon atoms and two triple bonds at positions 12 and 14.
Rarity
It is a rare and unique compound.
Biological and biomedical applications
HCA has potential applications in various fields due to its unique properties.
Antimicrobial properties
HCA has been shown to possess antimicrobial properties, making it a promising candidate for the development of new pharmaceuticals.
Antifungal properties
The compound also exhibits antifungal properties, which can be useful in treating fungal infections.
Antitumor properties
HCA has demonstrated antitumor properties, indicating its potential in cancer research and treatment.
Functional biomaterials
HCA has been investigated for its potential use in the fabrication of functional biomaterials, such as anti-fouling and anti-corrosive coatings.
Cellular processes regulation
The compound has been studied for its role in the regulation of cellular processes, including inflammation and immune response.
Industrial applications
HCA shows potential for various industrial applications, particularly in the development of new materials and coatings.
Medical applications
Due to its antimicrobial, antifungal, and antitumor properties, HCA has potential applications in the medical field for the development of new pharmaceuticals and treatments.
Scientific applications
The compound's unique properties and potential for regulating cellular processes make it an interesting subject for further scientific research and exploration.
Check Digit Verification of cas no
The CAS Registry Mumber 106510-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,1 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106510-41:
(8*1)+(7*0)+(6*6)+(5*5)+(4*1)+(3*0)+(2*4)+(1*1)=82
82 % 10 = 2
So 106510-41-2 is a valid CAS Registry Number.
106510-41-2Relevant articles and documents
Self-assembled nanotubes and helical tapes from diacetylene nonionic amphiphiles. Structural studies before and after polymerization
Perino, Aurelia,Schmutz, Marc,Meunier, Stephane,Mesini, Philippe J.,Wagner, Alain
, p. 12149 - 12155 (2011)
We synthesized new amphiphiles comprised of a single diacetylenic chain and an oligoethylenoxide polar chain linked by an amide bond. In aqueous medium, they are not soluble at room temperature but form weak gels. Electron microscopy studies have shown that they self-assemble into helical tapes or nanotubes with lengths of several micrometers, and inner and outer diameters of 50 ± 1 and 59 ± 1 nm, respectively. The wall has a thickness of 10 ± 1 nm for both kinds of objects and has an amphiphile bilayer structure. The hydrophobic chains are ordered, and the amide groups are linked with each other by H-bonds. The dissociation of the tubes is a first-order transition with an enthalpy of ca. 40 kJ mol-1. The nanotubes were photopolymerized to yield purple solutions consisting of helical tapes and almost flat ribbons. The polymers exhibit irreversible thermochromism upon heating.
Synthesis of Photopolymerizable Long-Chain Conjugated Diacetylenic Acids and Alcohols from Butadiyne Synthons
Xu, Zhenchun,Byun, Hoe-Sup,Bittman, Robert
, p. 7183 - 7186 (2007/10/02)
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