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2-Fluoropropan-1-ol, also known as 1-fluoropropan-2-ol, is a colorless liquid with a pungent odor. It is a fluorinated alcohol that serves as an important intermediate in the synthesis of various compounds, particularly in the pharmaceutical and agrochemical industries. Due to its unique chemical properties, it is also utilized as a solvent and a reagent in organic synthesis. However, it is highly flammable and poses potential health risks if not handled and stored properly, necessitating the implementation of appropriate safety measures.

3824-87-1

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3824-87-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoropropan-1-ol is used as a key intermediate in the production of pharmaceuticals for its ability to impart specific properties to the final drug molecules. Its fluorinated nature can enhance the lipophilicity, metabolic stability, and bioavailability of the resulting compounds, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Fluoropropan-1-ol is employed as an intermediate in the synthesis of various agrochemicals, including pesticides and herbicides. Its incorporation can improve the effectiveness and selectivity of these products, contributing to more efficient and targeted agricultural solutions.
Used as a Solvent in Organic Synthesis:
2-Fluoropropan-1-ol is utilized as a solvent in organic synthesis due to its ability to dissolve a wide range of organic compounds. Its unique properties as a fluorinated alcohol make it suitable for specific types of chemical reactions, facilitating the synthesis of complex organic molecules.
Used as a Reagent in Organic Synthesis:
As a reagent, 2-Fluoropropan-1-ol plays a crucial role in various organic reactions, such as nucleophilic substitutions and esterification processes. Its reactivity and selectivity can be tailored to achieve desired outcomes in the synthesis of specific organic compounds, making it a versatile tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 3824-87-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,2 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3824-87:
(6*3)+(5*8)+(4*2)+(3*4)+(2*8)+(1*7)=101
101 % 10 = 1
So 3824-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H7FO/c1-3(4)2-5/h3,5H,2H2,1H3

3824-87-1Relevant 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.

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