10519-17-2 Usage
Uses
Used in Fragrance Industry:
2-Undecynoic acid ethyl ester is used as a fragrance ingredient for its distinctive scent, contributing to the formulation of perfumes and personal care products. Its aromatic properties make it a valuable addition in creating complex and appealing fragrances.
Used in Polymer Production:
In the polymer industry, 2-Undecynoic acid ethyl ester serves as a building block for the synthesis of polymers. Its chemical structure allows it to be incorporated into polymer chains, potentially enhancing the properties of the resulting materials.
Used in Chemical Synthesis:
2-Undecynoic acid ethyl ester is utilized as a starting material in the synthesis of various compounds. Its reactivity and functional groups make it a versatile component in organic chemistry, facilitating the creation of a wide range of products.
Safety and Storage:
Due to its combustible nature and potential to cause skin and eye irritation, 2-Undecynoic acid ethyl ester should be handled with care. It must be stored in a cool, dry place, away from direct sunlight and sources of ignition to prevent accidents and ensure stability.
Check Digit Verification of cas no
The CAS Registry Mumber 10519-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,1 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10519-17:
(7*1)+(6*0)+(5*5)+(4*1)+(3*9)+(2*1)+(1*7)=72
72 % 10 = 2
So 10519-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O2/c1-3-5-6-7-8-9-10-11-12-13(14)15-4-2/h3-10H2,1-2H3
10519-17-2Relevant academic research and scientific papers
Structure-antitumor activity relationship of semi-synthetic spicamycin derivatives
Sakai,Kawai,Kamishohara,Odagawa,Suzuki,Uchida,Kawasaki,Tsuruo,Otake
, p. 1467 - 1480 (2007/10/03)
New derivatives of spicamycin modified at the fatty acid moieties of the molecule were synthesized and their structure-activity relationships were examined. The antitumor activity was greatly influenced by modification of the fatty acid moieties to tetradecadienoyl or dodecadienoyl analogues exhibiting better antitumor activity against COL-1 human colon cancer xenograft than SPM VIII.
