65031-95-0 Usage
Uses
Used in Adhesives Industry:
S-Glycidyl Acetate is used as a key component in the formulation of adhesives, leveraging its reactive nature to create strong bonds between various substrates. Its ability to engage in ring-opening reactions allows for the development of adhesives with tailored properties to suit specific applications.
Used in Coatings Industry:
In the coatings industry, S-Glycidyl Acetate is utilized as a critical ingredient to enhance the performance characteristics of coatings. Its reactivity contributes to the formation of durable and robust coatings with improved adhesion, chemical resistance, and mechanical strength.
Used in Resins Production:
S-Glycidyl Acetate is employed as a precursor in the synthesis of resins, which are essential materials in the manufacturing of composites, plastics, and other polymer-based products. Its incorporation into resins allows for the creation of materials with tailored properties, such as heat resistance, rigidity, and chemical stability.
Used in Polymer Synthesis:
As a versatile building block, S-Glycidyl Acetate is used in the synthesis of various polymers, where its reactivity enables the development of polymers with specific characteristics. These polymers find applications in a wide range of industries, including automotive, aerospace, electronics, and consumer goods.
Used in Pharmaceutical Industry:
S-Glycidyl Acetate is also utilized as an intermediate in the synthesis of pharmaceuticals, where its ability to undergo ring-opening reactions allows for the creation of complex molecular structures with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65031-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,3 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65031-95:
(7*6)+(6*5)+(5*0)+(4*3)+(3*1)+(2*9)+(1*5)=110
110 % 10 = 0
So 65031-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O3/c1-4(6)7-2-5-3-8-5/h5H,2-3H2,1H3/t5-/m1/s1
65031-95-0Relevant articles and documents
Continuous-Flow Synthesis of (R)-Propylene Carbonate: An Important Intermediate in the Synthesis of Tenofovir
Suveges, Nicolas S.,Rodriguez, Anderson A.,Diederichs, Carla C.,de Souza, Stefania P.,Le?o, Raquel A. C.,Miranda, Leandro S. M.,Horta, Bruno A. C.,Pedraza, Sérgio F.,de Carvalho, Otavio V.,Pais, Karla C.,Terra, José H. C.,de Souza, Rodrigo O. M. A.
supporting information, p. 2931 - 2938 (2018/06/27)
(R)-Propylene carbonate is an important intermediate in the synthesis of tenofovir pro-drugs such as tenofovir alafenamide fumarate (TAF) and tenofovir diisoproyl fumarate (TDF). Independent of the pro-drug type, tenofovir presents a chiral secondary hydroxy derivative, which can be obtained directly from (R)-propylene carbonate. Herein, we report our chemo-enzymatic continuous-flow strategy towards (R)-propylene carbonate starting from a very cheap and renewable raw material, glycerol. We were able to synthesize (R)-propylene carbonate in seven continuous-flow steps, starting from glycerol, in good-to-excellent yields (66–93 %) and excellent selectivity (E > 200).
A direct HPLC method for the determination of enantiomeric excess of some highly enantiomerically enriched derivatives of chiral glycidols
Chen, Jian
, p. 7663 - 7666 (2007/10/02)
A newly developed HPLC method which requires no derivatization is used to determine accurately the enantiomeric purity of some glycidol-based derivatives that have been enantiomerically enriched by recrystallization or lipase-catalyzed kinetic resolution after the Sharpless Asymmetric Epoxidation.
