17351-34-7 Usage
Uses
Used in Tissue Engineering Applications:
14-Pentadecenoic acid is used as a component in the fabrication of fibrous scaffold biomaterials for tissue engineering. Its incorporation into these scaffolds enhances their structural integrity and biocompatibility, making them suitable for supporting cell growth and tissue regeneration.
Used in Gas Chromatography:
In the field of analytical chemistry, 14-Pentadecenoic acid is used in the construction of metallomesogenic side-chain polymers that coat capillary columns used in gas chromatography. These polymers provide improved separation and detection of various compounds, making the analysis more accurate and reliable.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 14-Pentadecenoic acid may also have potential applications in the pharmaceutical industry, possibly as a precursor for the synthesis of various drugs or as an additive in the formulation of medications.
Check Digit Verification of cas no
The CAS Registry Mumber 17351-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,5 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17351-34:
(7*1)+(6*7)+(5*3)+(4*5)+(3*1)+(2*3)+(1*4)=97
97 % 10 = 7
So 17351-34-7 is a valid CAS Registry Number.
17351-34-7Relevant academic research and scientific papers
Enzymatic Oxidative Tandem Decarboxylation of Dioic Acids to Terminal Dienes
Dennig, Alexander,Kurakin, Sara,Kuhn, Miriam,Dordic, Andela,Hall, Mélanie,Faber, Kurt
supporting information, p. 3473 - 3477 (2016/07/29)
The biocatalytic oxidative tandem decarboxylation of C7–C18dicarboxylic acids to terminal C5–C16dienes was catalyzed by the P450 monooxygenase OleT with conversions up to 29 % for 1,11-dodecadiene (0.49 g L–1). The sequential nature of the cascade was proven by the fact that decarboxylation of intermediate C6–C11ω-alkenoic acids and heptanedioic acid exclusively gave nonconjugated 1,4-pentadiene; scale-up allowed the isolation of 1,15-hexadecadiene and 1,11-dodecadiene; the system represents a short and green route to terminal dienes from renewable dicarboxylic acids.
