2805-15-4 Usage
Uses
Used in Building Materials:
2,2,2-Trifluoroethyl phosphate is used as a flame retardant and plasticizer to enhance the safety and flexibility of building materials, thereby reducing the risk of fire and improving the durability of the products.
Used in Electronics:
In the electronics industry, 2,2,2-trifluoroethyl phosphate is employed as a flame retardant and plasticizer in various components, ensuring the safety and functionality of electronic devices by reducing the risk of fire and increasing the flexibility of materials.
Used in Upholstery:
2,2,2-Trifluoroethyl phosphate is used as a flame retardant and plasticizer in upholstery materials, providing fire safety and enhancing the flexibility and durability of furniture and other upholstered items.
Used as an Intermediate in Chemical Synthesis:
2,2,2-Trifluoroethyl phosphate serves as an important intermediate in the synthesis of other chemicals, contributing to the development of new compounds and materials with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2805-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2805-15:
(6*2)+(5*8)+(4*0)+(3*5)+(2*1)+(1*5)=74
74 % 10 = 4
So 2805-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C2H4F3O4P/c3-2(4,5)1-9-10(6,7)8/h1H2,(H2,6,7,8)
2805-15-4Relevant academic research and scientific papers
Evaluation of Natural and Synthetic Phosphate Donors for the Improved Enzymatic Synthesis of Phosphate Monoesters
Tasnádi, Gábor,Jud, Wolfgang,Hall, Mélanie,Baldenius, Kai,Ditrich, Klaus,Faber, Kurt
supporting information, p. 2394 - 2401 (2018/05/14)
Undesired product hydrolysis along with large amounts of waste in form of inorganic monophosphate by-product are the main obstacles associated with the use of pyrophosphate in the phosphatase-catalyzed synthesis of phosphate monoesters on large scale. In order to overcome both limitations, we screened a broad range of natural and synthetic organic phosphate donors with several enzymes on a broad variety of hydroxyl-compounds. Among them, acetyl phosphate delivered stable product levels and high phospho-transfer efficiency at the lower functional pH-limit, which translated into excellent productivity. The protocol is generally applicable to acid phosphatases and compatible with a range of diverse substrates. Preparative-scale transformations using acetyl phosphate synthesized from cheap starting materials yielded multiple grams of various sugar phosphates with up to 433 g L?1 h?1 space-time yield and 75% reduction of barium phosphate waste. (Figure presented.).
