71673-32-0 Usage
Uses
Used in Research Applications:
1,11-Hexadecadiyne is used as a research compound for the development of self-assembling monolayers and as a precursor for the synthesis of conjugated polymers. Its unique structure and properties make it a valuable tool in scientific investigations.
Used in Organic Electronics:
1,11-Hexadecadiyne is used as a material in the field of organic electronics due to its unique electronic properties. Its potential applications in this industry include the development of new electronic devices and components that leverage the compound's characteristics.
Used in Polymer Synthesis:
1,11-Hexadecadiyne is used as a precursor in the synthesis of conjugated polymers. Its ability to undergo polymerization and form long chains of carbon atoms makes it a useful building block for creating advanced polymer materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 71673-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,7 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71673-32:
(7*7)+(6*1)+(5*6)+(4*7)+(3*3)+(2*3)+(1*2)=130
130 % 10 = 0
So 71673-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H26/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h1H,4-9,11,13-16H2,2H3
71673-32-0Relevant academic research and scientific papers
Studies on the monoalkylation of terminal diynes
Pojar-Fene?an, Maria,Balea, Ana,Pop, Lidia,Oprean, Ioan,Grecu, Rodica
, p. 179 - 183 (2007/10/03)
In our study we intend to find out the favourable conditions for the monoalkylation of terminal diynes by following two reaction pathways. The reaction in DMSO, using dimsyl sodium as metallation reagent and butylbromide for the alkylation, gives up to 80% conversion of terminal diynes to their monoalkyl derivatives. Mass spectra of terminal diynes 1-4 and of the corresponding monobutyl 1a-4a and dibutyl 1b-4b diynes are given.
EXO- AND ENDOHORMONES. XIV. STEREOSPECIFIC SYNTHESIS OF 3Z, 13Z- AND 3E, 13E-3,13-OCTADECADIEN-1-YL ACETATE
Pop, Lidia,Pojar-Fenesan, Maria,Oprean, Ioan
, p. 453 - 456 (2007/10/02)
The two geometric isomers, 3Z, 13Z-, (I) and 3E, 13E-, (II), of 3,13-octadecadien-1-yl acetate, coponents of the phermonal lure of many lepidopteran insect species, were prepared in high isomeric purity by using 1,11-dodecadiine.
