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1-Fluoro-3-hydroxy-2-propanone, also known as fluoroacetate or fluoroacetone, is a halogenated organic compound with the chemical formula C3H5FO2. It is a colorless, volatile, and highly toxic liquid with a pungent odor. 1-Fluoro-3-hydroxy-2-propanone is a derivative of acetone, where one hydrogen atom is replaced by a fluorine atom, and a hydroxyl group is present at the 3-position. Due to its reactivity and toxicity, 1-fluoro-3-hydroxy-2-propanone is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fluorinated compounds. It is also known for its potential use as a biocidal agent. However, due to its hazardous nature, handling and storage of this chemical require strict safety measures and precautions.

62522-70-7

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62522-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62522-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,2 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62522-70:
(7*6)+(6*2)+(5*5)+(4*2)+(3*2)+(2*7)+(1*0)=107
107 % 10 = 7
So 62522-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H5FO2/c4-1-3(6)2-5/h5H,1-2H2

62522-70-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-3-hydroxypropan-2-one

1.2 Other means of identification

Product number -
Other names 2-Propanone,1-fluoro-3-hydroxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62522-70-7 SDS

62522-70-7Downstream Products

62522-70-7Relevant 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.

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