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3-(4-Chlorophenoxy)pentane-2,4-dione is a chemical compound characterized by its molecular formula C11H13ClO3. It is a yellow solid that serves as a versatile building block in the synthesis of a variety of organic compounds and pharmaceuticals. The presence of a chlorophenyl group in its structure makes it a valuable starting material for the preparation of other chlorinated organic compounds. Additionally, as a pentanedione derivative, it is recognized for its potential as a chelating agent in inorganic and bioinorganic chemistry. This chemical is notable for its potential applications in medicinal chemistry, drug development, and the synthesis of complex organic molecules for research.

31168-10-2

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31168-10-2 Usage

Uses

Used in Pharmaceutical Synthesis:
3-(4-Chlorophenoxy)pentane-2,4-dione is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be readily modified and incorporated into various drug molecules. Its unique structure allows for the development of new therapeutic agents with potential applications in treating a range of medical conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 3-(4-chlorophenoxy)pentane-2,4-dione is used as a starting material for the preparation of other chlorinated organic compounds. Its reactivity and functional groups make it suitable for a wide range of chemical reactions, facilitating the creation of complex organic molecules for research and industrial applications.
Used in Chelating Agent Development:
3-(4-Chlorophenoxy)pentane-2,4-dione is utilized as a chelating agent in inorganic and bioinorganic chemistry. Its pentanedione moiety provides the necessary functionality to form stable complexes with metal ions, which is crucial in various chemical processes and analytical techniques.
Used in Medicinal Chemistry Research:
In medicinal chemistry, 3-(4-chlorophenoxy)pentane-2,4-dione is employed as a structural component in the design and synthesis of new drug candidates. Its unique properties and reactivity contribute to the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Drug Development:
3-(4-chlorophenoxy)pentane-2,4-dione plays a role in drug development as a precursor to potential active pharmaceutical ingredients. Its chemical properties allow for the exploration of new drug scaffolds and the optimization of drug candidates to enhance their pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 31168-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31168-10:
(7*3)+(6*1)+(5*1)+(4*6)+(3*8)+(2*1)+(1*0)=82
82 % 10 = 2
So 31168-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11ClO3/c1-7(13)11(8(2)14)15-10-5-3-9(12)4-6-10/h3-6,11H,1-2H3

31168-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenoxy)pentane-2,4-dione

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:31168-10-2 SDS

31168-10-2Downstream Products

31168-10-2Relevant academic research and scientific papers

Synthesis and formulation of some new azines and evaluation of their fungicidal efficiency

Youssef,Ibrahim,Attia, Hanaa A.E.,Hamouda

scheme or table, p. 163 - 175 (2011/06/19)

TWENTY FIVE new 3-cyanopyridine-2(lH)-thione derivatives were synthesized by different routes. Structural elucidation of the prepared compounds was carried out by their correct elemental analyses as well as spectroscopic data (IR, Ms, 1Η-NMR). Fungicidal activity of the new compounds, on two soil borne fungi, was assayed by food poison technique where, some of the new compounds showed good fungicidal activity. Formulation of the most potent one, in the form of 20% EC, was carried out and its fungicidal activity was evaluated which was found to be more active than the standard fungicide Flutolanil (Moncut 25%WP).

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