143109-97-1 Usage
Uses
Used in Chemical Synthesis:
(R)-2-FLUOROPROPAN-1-OL, 97% MIN. is used as a reagent for the synthesis of other organic compounds, facilitating the creation of a diverse range of chemical products.
Used in Pharmaceutical Production:
(R)-2-FLUOROPROPAN-1-OL, 97% MIN. is used as an intermediate in the production of pharmaceuticals, contributing to the development of new medications and therapies.
Used in Agrochemical Production:
(R)-2-FLUOROPROPAN-1-OL, 97% MIN. is used as an intermediate in the production of agrochemicals, aiding in the development of more effective and environmentally friendly products for the agricultural industry.
Used in Organic Synthesis and Medicinal Chemistry:
(R)-2-FLUOROPROPAN-1-OL, 97% MIN. is used as a compound with potential applications in the field of organic synthesis and medicinal chemistry, where its unique properties can be leveraged to create novel compounds and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 143109-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,1,0 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143109-97:
(8*1)+(7*4)+(6*3)+(5*1)+(4*0)+(3*9)+(2*9)+(1*7)=111
111 % 10 = 1
So 143109-97-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H7FO/c1-3(4)2-5/h3,5H,2H2,1H3/t3-/m1/s1
143109-97-1Relevant articles and documents
Synthesis and Enantioselective Fluorodehydroxylation Reactions of (S)-2-(Methoxymethyl)pyrrolidin-1-ylsulphur Trifluoride, the First Homochiral Aminofluorosulphurane
Hann, Gerald L.,Sampson, Paul
, p. 1650 - 1651 (2007/10/02)
(S)-2-(Methoxymethyl)pyrrolidin-1-ylsulphur trifluoride (7), the first homochiral aminofluorosulphurane and one of the most stable aminofluorosulphuranes yet reported, has been prepared, and has been shown to be an effective enantioselective fluorohydroxylating agent.
REACTION OF HYDROXY AND CARBONYL COMPOUNDS WITH SULFUR TETRAFLUORIDE. XVI. REACTIONS OF VICINAL DIHYDRIC ALCOHOLS WITH SULFUR TETRAFLUORIDE
Burmakov, A. I.,Hassanein, Salah Mohamed,Kunshenko, B. V.,Alekseeva, L. A.,Yagupol'skii, L. M.
, p. 1146 - 1149 (2007/10/02)
During the action of sulfur tetrafluoride on ethanediol, d,l-1,2-propanediol, and d,l-3,3,3-trifluoro-1,2-propanediol regioselective substitution of one of the hydroxyl groups by a fluorine atom occurs, depending on the electronic nature of the groups present in the molecule.The second hydroxy group is converted into a fluorosulfite group.
