57395-49-0 Usage
General Description
10-Iodo-1-decanol, also known as decyl iodide, is a chemical compound with the molecular formula C10H21IO. It is a white to pale yellow solid with a faint odor, and it is used in organic synthesis as a starting material for the preparation of various iodinated compounds. This chemical is also utilized in the production of surfactants, lubricants, and other industrial applications. It has potential antifungal and antibacterial properties, and it may be used in pharmaceutical formulations and as a topical antiseptic. Additionally, 10-Iodo-1-decanol has been studied for its potential use in the development of new materials such as polymers and coatings. However, it is important to handle this chemical with care, as it is toxic if swallowed and can cause skin and eye irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 57395-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,9 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57395-49:
(7*5)+(6*7)+(5*3)+(4*9)+(3*5)+(2*4)+(1*9)=160
160 % 10 = 0
So 57395-49-0 is a valid CAS Registry Number.
57395-49-0Relevant articles and documents
New synthesis of (11Z,13Z)-11,13-Hexadecadienal, the female sex pheromone of the navel orangeworm
Mori, Kenji
experimental part, p. 2727 - 2730 (2010/09/11)
(11Z,13Z)-11,13-Hexadecadienal, the female sex pheromone of the navel orangeworm (Amyelois transitella), was synthesized from commercially available 10-bromo-1-decanol in a 27% overall yield (8 steps). The synthesis was achieved by using 10-iododecanal, trimethylsilylacetylene and (Z)-1-bromo-12-butene as the key building blocks, employing Sonogashira-Hagihara coupling and Brown's hydroboration-protonolysis as the key reactions. The terminal formyl group was installed in the earlier stage of the synthesis rather than in the final step. This procedure enabled the multi-gram-scale preparation of this economically important pheromone.
