1190-14-3 Usage
Uses
Used in Organic Synthesis:
(4-bromobutyl)phosphonic acid serves as a valuable building block in organic synthesis, contributing to the creation of complex organic molecules and compounds. Its reactivity and functional groups make it a key component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions as a Reagent:
As a reagent, (4-bromobutyl)phosphonic acid is utilized in a variety of chemical reactions to facilitate the formation of desired products. Its presence can enhance reaction efficiency and selectivity, making it an indispensable tool in the laboratory and industrial settings.
Used in Metal Chelation and Coordination Chemistry:
(4-bromobutyl)phosphonic acid is employed as a metal chelator and coordination compound due to its strong affinity for metal ions. This property is crucial in stabilizing metal complexes and has applications in areas such as catalysis, where metal complexes are often used to accelerate chemical reactions.
Used as a Corrosion Inhibitor:
In industrial applications, (4-bromobutyl)phosphonic acid functions as an effective corrosion inhibitor. It protects metal surfaces from degradation and wear, which is particularly important in industries that involve the use of metal components and structures exposed to harsh environments.
Used as a Stabilizer in Industrial Processes:
(4-bromobutyl)phosphonic acid also acts as a stabilizer in various industrial processes, enhancing the performance and longevity of products. Its stabilizing properties can prevent unwanted side reactions and degradation, ensuring the consistency and quality of the final products.
Used in Pharmaceuticals:
(4-bromobutyl)phosphonic acid holds potential in the pharmaceutical industry, where its unique chemical properties can be harnessed for the development of new drugs and therapeutic agents. Its ability to interact with metal ions may contribute to its use in medicinal chemistry.
Used in Agrochemicals:
Similarly, in agrochemicals, the compound may find applications in the development of new pesticides, herbicides, or other agricultural products. Its versatility and reactivity could lead to the creation of novel agrochemicals with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1190-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1190-14:
(6*1)+(5*1)+(4*9)+(3*0)+(2*1)+(1*4)=53
53 % 10 = 3
So 1190-14-3 is a valid CAS Registry Number.
1190-14-3Relevant academic research and scientific papers
Lee,Kepley,Hong,Akhter,Mallouk
, p. 2597 - 2601 (1988)
Multilayer films of zirconium 1,10-decanediylbis(phosphonate) have been prepared on silicon and gold substrates and characterized by ellipsometry, XPS, and electrochemical measurements. The deposition technique requires first covalent attachment or adsorption of a phosphonic acid anchoring agent. The functionalized substrates are exposed alternately to aqueous ZrOCl//2 and 1,10-decanediylbis(phosphonic acid) solutions to yield multilayer films. Ellipsometry shows an increase in film thickness, on Si, of 17 Angstrom/layer, which corresponds to the layer spacing in bulk Zr(O//3PC//1//0H//2//0PO//3). Variable take-off angle X-ray photoelectron spectra from four-layer films have attenuated Si peaks but strong Zr and P peaks when the detector is 70 degree off the surface normal, implying that the films on Si are continuous.
α-Zirconium phosphonates: Versatile supports for N-heterocyclic carbenes
Chessa, Simona,Clayden, Nigel J.,Bochmann, Manfred,Wright, Joseph A.
supporting information; experimental part, p. 797 - 799 (2009/07/10)
α-Zirconium phosphonates derivatised with N-heterocyclic carbenes provide a versatile platform for organocatalysis and metal-catalysed transformations, including the ring-opening polymerisation of cyclic esters, and olefin metathesis and hydroformylations by surface-bound ruthenium, rhodium and iridium complexes. The Royal Society of Chemistry.
