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3-(2-Fluorophenoxy)-1,2-propanediol is a synthetic organic compound characterized by its molecular formula C9H11FO3. It features a propanediol backbone with a fluorophenoxy group attached to the third carbon. This fluorinated derivative of a phenol ether is known for its unique chemical properties, which include a single fluorine atom in the ortho position relative to the hydroxyl group on the phenyl ring. The compound is of interest in various chemical and pharmaceutical applications due to its potential reactivity and the influence of the fluorine atom on its electronic and steric properties. It is often used as an intermediate in the synthesis of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals, where its unique characteristics can contribute to the desired activity of the final product.

399-28-0

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399-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 399-28-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 399-28:
(5*3)+(4*9)+(3*9)+(2*2)+(1*8)=90
90 % 10 = 0
So 399-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11FO3/c10-8-3-1-2-4-9(8)13-7(5-11)6-12/h1-4,7,11-12H,5-6H2

399-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-fluorophenoxy)propane-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,2-Dihydroxy-3-o-fluorphenoxypropan

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:399-28-0 SDS

399-28-0Downstream Products

399-28-0Relevant academic research and scientific papers

Crystallization of chiral compounds 3. 3-Phenoxypropane-1,2-diol and 3-(2-halophenoxy)propane-1,2-diols

Zakharychev,Lazarev,Bredikhina,Bredikhin

, p. 230 - 237 (2007/10/03)

Specific features of melting of crystalline samples of 3-(2-R-phenoxy) propane-1,2-diols with different enantiomeric compositions were studied by differential scanning calorimetry. The melting points and enthalpies of melting for the racemate and individual stereoisomers were determined. Binary phase diagrams were constructed. The entropy of mixing of individual enantiomers in the liquid phase and the free energy of formation of the racemic compound were calculated. The thermochemical data indicate that the racemates are formed upon the crystallization of phenoxy-and 2-fluorophenoxy-containing compounds, while crystallization of the chloro-, bromo-, and iodo-substituted analogs would form racemic conglomerates.

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