430-50-2 Usage
Uses
Used in Organic Synthesis:
1-Fluoro-2-propanol is used as a solvent for facilitating various chemical reactions in organic synthesis. Its ability to dissolve a wide range of compounds makes it a valuable asset in this field.
Used in Pharmaceutical Production:
1-Fluoro-2-propanol serves as an intermediate in the manufacturing process of pharmaceuticals. Its role is crucial for the synthesis of specific drug compounds, contributing to the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, 1-Fluoro-2-propanol is utilized as an intermediate. It plays a part in the creation of substances that help protect crops and enhance agricultural productivity.
Used in Dye Production:
1-Fluoro-2-propanol is used as a component in the production of dyes. Its chemical properties are instrumental in developing colorants for various applications.
Used in Coating Production:
1-FLUORO-2-PROPANOL is also employed in the creation of coatings, where it contributes to the formation of protective and decorative layers on different surfaces.
Used in Flavor Production:
1-Fluoro-2-propanol finds application in the flavor industry, where it is used to develop and enhance flavors for food and beverages.
Safety Considerations:
Despite its low toxicity, 1-Fluoro-2-propanol can cause irritation to the eyes, skin, and respiratory system if exposure to high levels occurs. Its highly flammable nature necessitates careful handling and storage in well-ventilated areas to prevent potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 430-50-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 430-50:
(5*4)+(4*3)+(3*0)+(2*5)+(1*0)=42
42 % 10 = 2
So 430-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H7FO/c1-3(5)2-4/h3,5H,2H2,1H3
430-50-2Relevant academic research and scientific papers
One-way biohydrogen transfer for oxidation of sec-alcohols
Lavandera, Ivan,Kern, Alexander,Resch, Verena,Ferreira-Silva, Bianca,Glieder, Anton,Fabian, Walter M. F.,De Wildeman, Stefaan,Kroutil, Wolfgang
supporting information; experimental part, p. 2155 - 2158 (2009/05/27)
(Chemical Equation Presented) Quasi-irreversible oxidation of sec-alcohols was achieved via biocatalytic hydrogen transfer reactions using alcohol dehydrogenases employing selected ketones as hydrogen acceptors, which can only be reduced but not oxidized. Thus, only 1 equiv of oxidant was required instead of a large excess. For the oxidation of both isomers of methylcarbinols a single nonstereoselective short-chain dehydrogenase/reductase from Sphingobium yanoikuyae was identified and overexpressed in E. coli.
Synthesis, biodistribution, and primate imaging of fluorine-18 labeled 2β-carbo-1'-fluoro-2-propoxy-3β-(4-chlorophenyl)tropanes. Ligands for the imaging of dopamine transporters by positron emission tomography
Xing, Dongxia,Chen, Ping,Keil, Robert,Kilts, Clinton D.,Shi, Bing,Camp, Vernon M.,Malveaux, Gene,Ely, Timothy,Owens, Michael J.,Votaw, John,Davis, Margaret,Hoffman, John M.,BaKay, Roy A. E.,Subramanian, Thygarajan,Watts, Ray L.,Goodman, Mark M.
, p. 639 - 648 (2007/10/03)
2β-(R)-Carbo-1-fluoro-2-propoxy-3β-(4-chlorophenyl)tropane ((R)-FIPCT, R-6) and 2β-(S)-carbo-1-fluoro-2-propoxy-3β-(4-chlorophenyl)tropane ((S)- FIPCT, S-6) were prepared and evaluated in vitro and in vivo for dopamine transporter (DAT) selectivity and sp
