100912-15-0 Usage
General Description
3-Methyl-1-tridecyn-3-ol is a chemical compound with the formula C14H27OH. It is a long-chain fatty alcohol derived from natural sources such as plants and animals. 3-METHYL-1-TRIDECYN-3-OL is commonly used in the production of perfumes, fragrances, and flavors due to its pleasant odor and ability to enhance the overall scent profile. In addition, it has been found to have insecticidal properties, making it useful in the formulation of insect repellents and pesticides. 3-Methyl-1-tridecyn-3-ol has also been studied for its potential applications in the medical field, particularly in the development of antimicrobial agents and pharmaceuticals. Overall, this chemical compound has a variety of industrial and commercial uses, owing to its unique properties and potential benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 100912-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100912-15:
(8*1)+(7*0)+(6*0)+(5*9)+(4*1)+(3*2)+(2*1)+(1*5)=70
70 % 10 = 0
So 100912-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O/c1-4-6-7-8-9-10-11-12-13-14(3,15)5-2/h2,15H,4,6-13H2,1,3H3
100912-15-0Relevant articles and documents
Ligand-Controlled Palladium-Catalyzed Carbonylation of Alkynols: Highly Selective Synthesis of α-Methylene-β-Lactones
Beller, Matthias,Ge, Yao,Jackstell, Ralf,Jiao, Haijun,Liu, Jiawang,Spannenberg, Anke,Yang, Ji,Ye, Fei
supporting information, p. 21585 - 21590 (2020/09/23)
The first general and regioselective Pd-catalyzed cyclocarbonylation to give α-methylene-β-lactones is reported. Key to the success for this process is the use of a specific sterically demanding phosphine ligand based on N-arylated imidazole (L11) in the presence of Pd(MeCN)2Cl2 as pre-catalyst. A variety of easily available alkynols provide under additive-free conditions the corresponding α-methylene-β-lactones in moderate to good yields with excellent regio- and diastereoselectivity. The applicability of this novel methodology is showcased by the direct carbonylation of biologically active molecules including natural products.
