2411-58-7 Usage
Description
Undecyl isocyanate, also known as n-undecylisocyanate, is an alkyl isocyanate compound that can be synthesized by reacting lauroyl chloride with sodium azide. It is a versatile chemical intermediate with potential applications in various industries due to its unique chemical properties.
Uses
Used in Polymer Synthesis:
Undecyl isocyanate is used as a monomer for the synthesis of poly(n-undecyl isocyanate) (PUDIC). This polymer has potential applications in the field of materials science, particularly in the development of new polymers with specific properties tailored for various uses.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, undecyl isocyanate is used as a key intermediate in the synthesis of starch-N-undecyl carbamate. UNDECYL ISOCYANATE has potential applications in drug delivery systems, where it can be used to improve the solubility, stability, and bioavailability of various pharmaceutical agents.
Used in Chemical Synthesis:
Undecyl isocyanate can also be used as a chemical intermediate in the synthesis of various other compounds, including those with potential applications in the coatings, adhesives, and elastomers industries. Its unique chemical properties make it a valuable building block for the development of new materials with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 2411-58-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2411-58:
(6*2)+(5*4)+(4*1)+(3*1)+(2*5)+(1*8)=57
57 % 10 = 7
So 2411-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H23NO/c1-2-3-4-5-6-7-8-9-10-11-13-12-14/h2-11H2,1H3
2411-58-7Relevant articles and documents
The mechanism of dephosphorylation of bis(2,4-dinitrophenyl) phosphate in mixed micelles of cationic surfactants and lauryl hydroxamic acid
Silva, Marcelo,Mello, Renata S.,Farrukh, M. Akhyar,Venturini, Janio,Bunton, Clifford A.,Milagre, Humberto M. S.,Eberlin, Marcos N.,Fiedler, Haidi D.,Nome, Faruk
supporting information; experimental part, p. 8254 - 8260 (2010/02/28)
(Figure Presented) Mixed micelles of cetyltrimethylammonium bromide (CTABr) or dodecyltrimethylammonium bromide (DTABr) and the α-nucleophile, lauryl hydroxamic acid (LHA) accelerate dephosphorylation of bis(2,4-dinitrophenyl) phosphate (BDNPP) over the pH range 4-10. With a 0.1 mole fraction of LHA in DTABr or CTABr, dephosphorylation of BDNPP is approximately 104-fold faster than its spontaneous hydrolysis, and monoanionic LHA- is the reactive species. The results are consistent with a mechanism involving concurrent nucleophilic attack by hydroxamate ion (i) on the aromatic carbon, giving an intermediate that decomposes to undecylamine and 2,4-dinitrophenol, and (ii) at phosphorus, giving an unstable intermediate that undergoes a Lossen rearrangement yielding a series of derivatives including N,N-dialkylurea, undecylamine, undecyl isocyanate, and carbamyl hydroxamate.
