62741-32-6 Usage
Uses
Used in Pharmaceutical Industry:
2,2-Dimethoxy-3-fluoro-1-propanol is used as a solvent and intermediate for the synthesis of various pharmaceutical compounds. Its properties make it suitable for use in the development of new drugs and the improvement of existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2-Dimethoxy-3-fluoro-1-propanol is employed as a solvent and intermediate in the production of pesticides and other agrochemicals. Its ability to dissolve a wide range of substances contributes to the effectiveness of these products.
Used in Chemical Production:
2,2-Dimethoxy-3-fluoro-1-propanol is used as a solvent and intermediate in the synthesis of various chemicals, including specialty plastics and coatings. Its versatility and properties make it a valuable component in the production of these materials.
Used in Specialty Plastics and Coatings Manufacturing:
2,2-Dimethoxy-3-fluoro-1-propanol is used as a key component in the manufacturing process of specialty plastics and coatings. Its unique properties contribute to the development of high-quality and durable products with specific applications.
Safety Precautions:
Due to its flammable nature and potential to cause irritation to the skin, eyes, and respiratory system, it is crucial to follow proper handling and storage procedures when working with 2,2-Dimethoxy-3-fluoro-1-propanol. This ensures the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 62741-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,4 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62741-32:
(7*6)+(6*2)+(5*7)+(4*4)+(3*1)+(2*3)+(1*2)=116
116 % 10 = 6
So 62741-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H11FO3/c1-8-5(3-6,4-7)9-2/h7H,3-4H2,1-2H3
62741-32-6Relevant academic research and scientific papers
Synthesis and Properties of Halohydroxyacetones and Halomethylglyoxals
Chari, Ravi V.J.,Kozarich, John W.
, p. 2355 - 2358 (2007/10/02)
A short, high-yield synthetic scheme for the preparation of halohydroxyacetones (4) and halomethylglyoxals (6) from the corresponding 3-halopyruvic acids is described.The key intermediate to both classes is the dimethyl ketal (3) of the halohydroxyacetone (4).The ketal alkohol (3) may be hydrolyzed to 4 or oxidized to the corresponding aldehyde (5) which, in turn, may be hydrolyzed to the halomethylglyoxal (6).Halohydroxyacetones (4) exist in solution as an equilibrium mixture of the free ketone and hydrate.Halomethylglyoxals (6) occur nearly exclusively as the dihydrates species.Some other properties of these compounds are described.
