125070-38-4 Usage
Uses
Used in Chemical Synthesis:
4,4,5,5,6,6,7,7,7-Nonafluoroheptane-1,2-diol is used as a building block in the chemical synthesis industry for creating other fluorochemicals. Its unique structure and stability contribute to the development of a wide range of products with specific applications.
Used in Surfactant Production:
In the surfactant industry, 4,4,5,5,6,6,7,7,7-Nonafluoroheptane-1,2-diol is used as a key component in the production of surfactants. Its surfactant properties allow it to function as a wetting agent or emulsifier, enhancing the performance of various formulations.
Used in Polymer Synthesis:
4,4,5,5,6,6,7,7,7-Nonafluoroheptane-1,2-diol is also utilized in the polymer industry as a monomer for the synthesis of polymers with specific properties. The incorporation of 4,4,5,5,6,6,7,7,7-NONAFLUOROHEPTANE-1,2-DIOL into polymer structures can result in materials with improved thermal and chemical resistance.
Used in Industrial Applications:
Due to its excellent chemical and thermal stability, 4,4,5,5,6,6,7,7,7-Nonafluoroheptane-1,2-diol finds use in various industrial applications where such properties are required. Its versatility makes it suitable for a broad spectrum of uses, from coatings to specialized fluids.
Environmental and Health Considerations:
While 4,4,5,5,6,6,7,7,7-Nonafluoroheptane-1,2-diol offers numerous benefits, its potential environmental and health effects are still under investigation. As a result, it is essential to exercise caution in its handling and use, ensuring that proper safety measures are in place to minimize any potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 125070-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,7 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125070-38:
(8*1)+(7*2)+(6*5)+(5*0)+(4*7)+(3*0)+(2*3)+(1*8)=94
94 % 10 = 4
So 125070-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7F9O2/c8-4(9,1-3(18)2-17)5(10,11)6(12,13)7(14,15)16/h3,17-18H,1-2H2
125070-38-4Relevant academic research and scientific papers
Chemistry of [(perfluoroalkyl)methyl] oxiranes. Regioselectivity of ring opening with O-nucleophiles and the preparation of amphiphilic monomers
Cirkva, Vladimir,Ameduri, Bruno,Boutevin, Bernard,Paleta, Oldrich
, p. 53 - 61 (2007/10/03)
The reactions of oxiranes RFCH2CH(-O-)CH2 (RF≡C4F9, C6F13, C8F17; 4a-4c) with a series of alkanols in the presence of a Lewis acid took place at the terminal carbon atom with complete regioselectivity. 2-Hydroxyethyl methacrylate and acrylate reacted similarly. The reaction with alkane diols was controlled to proceed with one or two molecules of the oxiranes chemoselectively. Non-regioselective, base-catalysed ring opening by methacrylic acid (83% terminal attack) was discussed on the basis of the hard and soft acids and bases (HSAB) concept. A convenient transformation of the oxiranes to the corresponding diols 13a-13c via dioxolane intermediates, and their conversion to bis-methacrylates, was accomplished with overall yields of 75%-79%. Thiourea converted the oxiranes into the corresponding thiiranes (15a-15c). The reactions afforded products generally in yields of 82%-98%.
