59287-65-9 Usage
Uses
Used in Adhesives Industry:
3-(oxiran-2-yl)propyl acetate is used as a reactive diluent for the production of epoxy resins, which are essential components in the formulation of high-performance adhesives. These adhesives are known for their strong bonding capabilities and resistance to various environmental factors, making them suitable for a wide range of applications.
Used in Coatings Industry:
In the coatings industry, 3-(oxiran-2-yl)propyl acetate is used as a reactive diluent in the production of epoxy resins. These resins contribute to the formation of durable and protective coatings that are resistant to chemicals, moisture, and abrasion. They are commonly used in automotive, marine, and industrial coatings.
Used in Composites Industry:
3-(oxiran-2-yl)propyl acetate is utilized as a reactive diluent in the manufacturing of epoxy resins for composite materials. These composites are known for their high strength-to-weight ratio, making them ideal for applications in aerospace, automotive, and construction industries.
Used as a Solvent:
3-(oxiran-2-yl)propyl acetate is used as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. Its solubility properties make it a valuable component in the formulation of cleaning agents, degreasers, and other industrial applications.
Used as an Intermediate:
In chemical synthesis, 3-(oxiran-2-yl)propyl acetate serves as an intermediate for the production of various chemicals and polymers. Its reactive nature allows it to be easily incorporated into complex chemical structures, making it a useful building block in the synthesis of specialty chemicals.
Used in Chemical Synthesis:
3-(oxiran-2-yl)propyl acetate is employed in chemical synthesis for the production of a variety of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its versatility and reactivity make it a valuable component in the synthesis of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 59287-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,8 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59287-65:
(7*5)+(6*9)+(5*2)+(4*8)+(3*7)+(2*6)+(1*5)=169
169 % 10 = 9
So 59287-65-9 is a valid CAS Registry Number.
59287-65-9Relevant academic research and scientific papers
Olefin epoxidation with bis(trimethylsilyl) peroxide catalyzed by inorganic oxorhenium derivatives. Controlled release of hydrogen peroxide
Yudin,Chiang,Adolfsson,Copéret
, p. 4713 - 4718 (2007/10/03)
The replacement of organometallic rhenium species (e.g., CH3ReO3) by less expensive and more readily available inorganic rhenium oxides (e.g., Re2O7, ReO3(OH), and ReO3) can be accomplished using bis(trimethylsilyl) peroxide (BTSP) as oxidant in place of aqueous H2O2. Using a catalytic amount of a proton source, controlled release of hydrogen peroxide helps preserve sensitive peroxorhenium species and enables catalytic turnover to take place. Systematic investigation of the oxorhenium catalyst precursors, substrate scope, and effects of various additives on olefin epoxidation with BTSP are reported in this contribution.
A simple and efficient method for epoxidation of terminal alkenes
Coperet, Christophe,Adolfsson, Hans,Sharpless, K. Barry
, p. 1565 - 1566 (2007/10/03)
The use of a catalytic amount of 3-cyanopyridine in the methyltrioxorhenium catalysed epoxidation of terminal alkenes with aqueous hydrogen peroxide speeds turnover, which results in the formation of many functionalized epoxides in high yields.
Metalloporphyrin-catalysed Epoxidation of Terminal Aliphatic Olefins with Hypochlorite Salts or Potassium Hydrogen Persulphate
Poorter, Bertha De,Meunier, Bernard
, p. 1735 - 1740 (2007/10/02)
Substitution of tetraphenylporphyrinatomanganese(III) complexes on the peripheral phenyl groups makes these compounds suitable as catalysts for the epoxidation of terminal olefins with mono-oxygen donors such as a sodium or lithium hypochlorite and potass
CATALYTIC EPOXIDATION OF ALIPHATIC TERMINAL OLEFINS WITH SODIUM HYPOCHLORITE
Poorter, Bertha de,Meunier, Bernard
, p. 1895 - 1896 (2007/10/02)
Meso-tetra(halogenophenyl)porphyrinatomanganese complexes catalyze the epoxidation of terminal olefins by sodium hypochlorite at room temperature; moderate to good yields of epoxides are obtained.
