28393-00-2 Usage
Chemical structure
10,12-Heneicosadiynoic acid is a long-chain fatty acid with 21 carbons and two triple bonds at positions 10 and 12.
Classification
It is a polyunsaturated fatty acid.
Source
It is found in fish and marine oils.
Therapeutic and pharmaceutical applications
It has been investigated for its potential therapeutic and pharmaceutical applications.
Anti-inflammatory properties
Studies have shown that 10,12-Heneicosadiynoic acid exhibits anti-inflammatory properties.
Anti-tumor properties
It has also been shown to have anti-tumor properties.
Potential for drug development
It is a promising candidate for the development of new drugs for various diseases.
Antimicrobial properties
It has been found to have antimicrobial properties.
Antifungal properties
It has also been found to have antifungal properties.
Versatility
10,12-Heneicosadiynoic acid is a valuable and versatile chemical compound.
Biological activities
It has significant biological activities.
Medical applications
It has potential medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28393-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,9 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28393-00:
(7*2)+(6*8)+(5*3)+(4*9)+(3*3)+(2*0)+(1*0)=122
122 % 10 = 2
So 28393-00-2 is a valid CAS Registry Number.
28393-00-2Relevant articles and documents
Plenty of Room at the Top: A Multi-Scale Understanding of nm-Resolution Polymer Patterning on 2D Materials
Brooks, Jacob T.,Claridge, Shelley A.,Davis, Tyson C.,Hayes, Tyler R.,Shi, Anni,Singh, Anamika,Villarreal, Terry A.
supporting information, p. 25436 - 25444 (2021/10/29)
Lamellar phases of alkyldiacetylenes in which the alkyl chains lie parallel to the substrate represent a straightforward means for scalable 1-nm-resolution interfacial patterning. This capability has the potential for substantial impacts in nanoscale electronics, energy conversion, and biomaterials design. Polymerization is required to set the 1-nm functional patterns embedded in the monolayer, making it important to understand structure–function relationships for these on-surface reactions. Polymerization can be observed for certain monomers at the single-polymer scale using scanning probe microscopy. However, substantial restrictions on the systems that can be effectively characterized have limited utility. Here, using a new multi-scale approach, we identify a large, previously unreported difference in polymerization efficiency between the two most widely used commercial diynoic acids. We further identify a core design principle for maximizing polymerization efficiency in these on-surface reactions, generating a new monomer that also exhibits enhanced polymerization efficiency.
