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1,1-Diethoxypentane-2,4-dione is a colorless, oily liquid chemical compound with the molecular formula C9H16O3. It is a derivative of 1,3-cyclohexanedione and is synthesized by the reaction of 1,3-cyclohexanedione with ethanol in the presence of an acid catalyst. 1,1-Diethoxypentane-2,4-dione is known for its use as a solvent in various industrial applications and in the synthesis of pharmaceuticals and agrochemicals. Due to its flammable nature, it should be handled with caution.

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  • 124237-06-5 Structure
  • Basic information

    1. Product Name: 1,1-Diethoxypentane-2,4-dione
    2. Synonyms: 1,1-Diethoxypentane-2,4-dione;1,1-Diethoxy-2,4-pentanedione;1,1-diethoxyacetylacetone
    3. CAS NO:124237-06-5
    4. Molecular Formula: C9H16O4
    5. Molecular Weight: 188.22094
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124237-06-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 283℃
    3. Flash Point: 121℃
    4. Appearance: /
    5. Density: 1.020
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,1-Diethoxypentane-2,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-Diethoxypentane-2,4-dione(124237-06-5)
    11. EPA Substance Registry System: 1,1-Diethoxypentane-2,4-dione(124237-06-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124237-06-5(Hazardous Substances Data)

124237-06-5 Usage

Uses

Used in Solvent Applications:
1,1-Diethoxypentane-2,4-dione is used as a solvent in various industrial applications due to its ability to dissolve a wide range of substances. Its solubility properties make it suitable for use in processes that require the dissolution of solids, liquids, or gases.
Used in Pharmaceutical Synthesis:
1,1-Diethoxypentane-2,4-dione is used as an intermediate in the synthesis of pharmaceuticals. Its unique chemical structure allows it to participate in various chemical reactions, contributing to the production of different medicinal compounds.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1,1-Diethoxypentane-2,4-dione is utilized as a precursor in the synthesis of various agrochemicals. Its involvement in the production process helps in creating effective compounds for agricultural applications, such as pesticides and herbicides.
Used in Chemical Research:
1,1-Diethoxypentane-2,4-dione is also used in chemical research for studying its properties and potential applications. Researchers explore its reactivity, stability, and interactions with other compounds to gain insights into its behavior and possible uses in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 124237-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,2,3 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124237-06:
(8*1)+(7*2)+(6*4)+(5*2)+(4*3)+(3*7)+(2*0)+(1*6)=95
95 % 10 = 5
So 124237-06-5 is a valid CAS Registry Number.

124237-06-5SDS

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 1,1-diethoxypentane-2,4-dione

1.2 Other means of identification

Product number -
Other names 1,1-diethoxy-pentane-2,4-dione

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:124237-06-5 SDS

124237-06-5Relevant articles and documents

Compounds Based on a Triethyl- or Trimethoxybenzene Scaffold Bearing Pyrazole, Pyridine, and Pyrimidine Groups: Syntheses and Representative Binding Studies towards Carbohydrates

Koch, Niklas,Seichter, Wilhelm,Mazik, Monika

, p. 2757 - 2767 (2016/08/31)

Pyrazole-based artificial receptors have often been used in the recognition of ions, but in the area of sugar recognition the potential of pyrazole-based recognition groups has only been rarely examined. In this paper we describe the syntheses of twelve n

Intramolecular [3+2] nitrile oxide cycloaddition: Synthesis of tetrahydroisoxazoloindazoles

Park, Kyung-Ho,Marshall, Will J.

, p. 4931 - 4934 (2007/10/03)

Novel tetrahydroisoxazoloindazoles were synthesized from substituted 1,3-diketones by employing intramolecular [3+2] nitrile oxide cycloaddition [INOC] reaction to alkene as the key step.

Pyrimidinylimidazole inhibitors of CSBP/P38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes

Adams, Jerry L.,Boehm, Jeffrey C.,Kassis, Shouki,Gorycki, Peter D.,Webb, Edward F.,Hall, Ralph,Sorenson, Margaret,Lee, John C.,Ayrton, Andrew,Griswold, Don E.,Gallagher, Timothy F.

, p. 3111 - 3116 (2007/10/03)

Pyrimidine analogs of the pyridinylimidazole class of CSBP/p38 kinase inhibitors were prepared in an effort to reduce the potent inhibition of hepatic cytochrome P450 observed for the pyridinyl compounds. The substitution of pyrimidin-4-yl, 2-methoxypyrimidin-4-yl, or 2- methylaminopyrimidin-4-yl for pyridin-4-yl effectively dissociates CSBP/p38 kinase from P450 inhibition for this series and furthermore achieves an increase in oral activity.

Porphyrins with four azole substituents in meso positions: X-ray crystal structure of meso-tetrakis-(1-benzylpyrazol-4-yl)-porphyrin at 200 K

Werner, Andreas,Sanchez-Migallon, Ana,Fruchier, Alain,Elguero, Jose,Fernandez-Castano, Cristina,Foces-Foces, Concepcion

, p. 4779 - 4800 (2007/10/02)

Several new porphyrins have been prepared in improved yields using an established method which was adapted to formylpyrazoles bearing on the pyrazole N1-nitrogen protective groups. The deprotection of N-para-methoxybenzyl and SEM protected meso

Substituted pyridine derivatives and pesticides containing them

-

, (2008/06/13)

Substituted pyridine compounds of formula I STR1 and plant-tolerated acid addition salts and metal salt complexes thereof, and fungicides containing these compounds.

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