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CAS

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792-57-4

Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)-, also known as 1-(3,4-dimethoxyphenyl)-2-(3-methoxyphenyl)ethanone, is an organic compound with the molecular formula C16H18O4. It is a derivative of acetophenone, featuring two phenyl rings, one with a 3,4-dimethoxy substitution and the other with a 3-methoxy substitution. Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)- is characterized by its aromatic structure and the presence of methoxy groups, which contribute to its chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. The compound's structure and functional groups make it a subject of interest for researchers studying the synthesis and properties of aromatic ketones.

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  • 792-57-4 Structure

  • Basic information

    1. Product Name: Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)-
    2. Synonyms:
    3. CAS NO:792-57-4
    4. Molecular Formula: C16H16O4
    5. Molecular Weight: 272.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 792-57-4.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: Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)-(792-57-4)
    11. EPA Substance Registry System: Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)-(792-57-4)

  • 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: 792-57-4(Hazardous Substances Data)

792-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 792-57-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 792-57:
(5*7)+(4*9)+(3*2)+(2*5)+(1*7)=94
94 % 10 = 4
So 792-57-4 is a valid CAS Registry Number.

792-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4-dimethoxyphenyl)-(3-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names Methanone, (3,4-dimethoxyphenyl)(3-methoxyphenyl)-

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:792-57-4 SDS

792-57-4Relevant articles and documents

Diphenylethylene compounds and uses thereof

-

, (2008/06/13)

The present invention relates to Diphenylethylene Compounds and compositions comprising a Diphenylethylene Compound. The present invention also relates to methods for preventing or treating various diseases and disorders by administering to a subject in need thereof one or more Diphenylethylene Compounds. In particular, the invention relates to methods for preventing or treating cancer or an inflammatory disorder by administering to a subject in need thereof one or more Diphenylethylene Compounds. The present invention further relates to articles of manufacture and kits comprising one or more Diphenylethylene Compounds.

Rapid microwave-promoted synthesis of functionalised benzophenones

Learmonth, David A.

, p. 2757 - 2762 (2007/10/03)

Several functionalised benzophenone derivatives have been conveniently obtained in moderate to good yield via the rapid, microwave-promoted Friedel-Crafts acylation of activated arenes with benzoic acids in polyphosphoric acid medium.

BeCl2 as a new highly selective reagent for dealkylation of aryl-methyl ethers

Sharghi, Hashem,Tamaddon, Fatemeh

, p. 13623 - 13640 (2007/10/03)

An efficient and simple method is introduced for the selective removal of methyl group from poly aryl-methyl ethers, in some important derivatives of benzophenones, xanthones, anthraquinones, aryl esters, benzamides and nitroanisoles with BeCl2.

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