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Ethanone, 1-[4-(diethoxymethyl)phenyl]-, is a chemical compound with the molecular formula C14H18O3. It is a derivative of ethanone, or acetone, featuring a substituted phenyl group with diethoxymethyl groups attached at the para position. Ethanone, 1-[4-(diethoxymethyl)phenyl]is characterized by its potential utility in organic synthesis and as a building block for more complex molecules due to the presence of the diethoxymethyl group.

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  • 125532-06-1 Structure
  • Basic information

    1. Product Name: Ethanone, 1-[4-(diethoxymethyl)phenyl]-
    2. Synonyms:
    3. CAS NO:125532-06-1
    4. Molecular Formula: C13H18O3
    5. Molecular Weight: 222.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125532-06-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanone, 1-[4-(diethoxymethyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-[4-(diethoxymethyl)phenyl]-(125532-06-1)
    11. EPA Substance Registry System: Ethanone, 1-[4-(diethoxymethyl)phenyl]-(125532-06-1)
  • 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: 125532-06-1(Hazardous Substances Data)

125532-06-1 Usage

Uses

Used in Pharmaceutical Synthesis:
Ethanone, 1-[4-(diethoxymethyl)phenyl]is utilized as a precursor in the synthesis of pharmaceuticals. Its unique structure allows for the creation of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Production:
Ethanone, 1-[4-(diethoxymethyl)phenyl]also serves as a precursor in the production of agrochemicals, playing a role in the development of pesticides, herbicides, and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Polymer Production:
Ethanone, 1-[4-(diethoxymethyl)phenyl]is employed in the manufacturing of polymers, which are large molecules composed of repeating structural units. Its incorporation into polymer chemistry can lead to the development of new materials with specific properties for various applications.
Used as a Solvent in Chemical Reactions:
In the chemical industry, this compound functions as a solvent, facilitating various chemical reactions. Its properties make it suitable for use in processes that require a stable and effective medium to carry out reactions smoothly.
Used in Organic Synthesis:
Ethanone, 1-[4-(diethoxymethyl)phenyl]is a valuable building block in organic synthesis, enabling the construction of more complex molecules with diverse applications across different industries, including pharmaceuticals, materials science, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 125532-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125532-06:
(8*1)+(7*2)+(6*5)+(5*5)+(4*3)+(3*2)+(2*0)+(1*6)=101
101 % 10 = 1
So 125532-06-1 is a valid CAS Registry Number.

125532-06-1SDS

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 1-[4-(diethoxymethyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 4'-diethylacetal-acetophenone

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:125532-06-1 SDS

125532-06-1Relevant articles and documents

Palladium-catalyzed acetylation of arenes

Ramgren, Stephen D.,Garg, Neil K.

supporting information, p. 824 - 827 (2014/03/21)

A simple method for the preparation of aryl methyl ketones is reported. The transformation involves the Pd-catalyzed coupling of an acyl anion equivalent, acetyltrimethylsilane, with aryl bromides to afford the corresponding acetylated arenes in synthetically useful yields. The methodology is tolerant of heterocycles and provides a new method for arene functionalization.

Polyfunctional phosphine ligands. Preparation of 4'-formyl-2-diphenylphosphinoacetophenone and its coordination properties

Soulivong, Daravong,Ziessel, Raymond,Matt, Dominique

, p. 207 - 216 (2007/10/02)

The trifunctional ligand C(O)CH2PPh2 (5) has been prepared in four steps (overall yield 50percent) starting from terephthalaldehyde mono-(diethylacetal) (1): reaction of 1 with CH3MgBr gives C6H4>CH(OH)CH3 (2).This is oxidize

Synthesis and coordination properties of novel polyfunctional phosphine ligands

Soulivong, Daravong,Matt, Dominique,Ziessel, Raymond,Douce, Laurent,Deschenaux, Robert

, p. 1151 - 1154 (2007/10/02)

4′-formyl-2-diphenylphosphino-acetophenone 5 has been prepared in four steps (50%) starting from terephtalaldehyde mono-(diethylacetal) 1. Condensation of 5 with the para-substituted anilines H2NA-i gives quantitatively the phosphine-imines 6-8

Novel Thiazolidine-2,4-diones as Potent Euglycemic Agents

Hulin, Bernard,Clark, David A.,Goldstein, Steven W.,McDermott, Ruth E.,Dambek, Paul J.,et al.

, p. 1853 - 1864 (2007/10/02)

A new series of thiazolidine-2,4-diones was obtained by replacing the ether function of englitazone with various functional groups, i.e., a ketone, alcohol, or olefin moiety.These compounds lower blood glucose levels in the genetically obese and insulin-r

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