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CAS

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1655-72-7

1-(4-Methoxyphenoxy)-2-methoxybenzene, also known as Anisole, is a colorless liquid chemical compound with the molecular formula C14H14O3. It is commonly used as a precursor in the synthesis of various organic compounds and serves as a versatile solvent in chemical reactions.

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  • 1655-72-7 Structure

  • Basic information

    1. Product Name: 1-(4-Methoxyphenoxy)-2-methoxybenzene
    2. Synonyms: 1-(4-Methoxyphenoxy)-2-methoxybenzene;1-Methoxy-2-(4-methoxyphenoxy)benzene;Benzene, 1-Methoxy-2-(4-Methoxyphenoxy)-
    3. CAS NO:1655-72-7
    4. Molecular Formula: C14H14O3
    5. Molecular Weight: 230.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1655-72-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(4-Methoxyphenoxy)-2-methoxybenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Methoxyphenoxy)-2-methoxybenzene(1655-72-7)
    11. EPA Substance Registry System: 1-(4-Methoxyphenoxy)-2-methoxybenzene(1655-72-7)

  • 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: 1655-72-7(Hazardous Substances Data)

1655-72-7 Usage

Uses

Used in Chemical Synthesis:
Anisole is used as a precursor in the synthesis of various organic compounds, making it an essential component in the production of a wide range of chemical products.
Used in Solvent Applications:
Anisole is utilized as a solvent in various chemical reactions due to its ability to dissolve a broad spectrum of substances, contributing to the efficiency and effectiveness of these processes.
Used in Fragrance and Perfume Industry:
Anisole is found in some fragrances and perfumes, where its sweet, pleasant odor adds to the overall scent profile of these products.
Used in Pharmaceutical Production:
Anisole is used in the production of pharmaceuticals, playing a crucial role in the development and manufacturing of various medications.
Used in Agrochemical Production:
Anisole is also used in the production of agrochemicals, contributing to the development of products that support agricultural practices and crop protection.
Used in Dye Production:
Anisole is utilized in the production of dyes, where its chemical properties aid in the creation of a diverse range of colorants for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1655-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1655-72:
(6*1)+(5*6)+(4*5)+(3*5)+(2*7)+(1*2)=87
87 % 10 = 7
So 1655-72-7 is a valid CAS Registry Number.

1655-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-2-(4-methoxyphenoxy)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1-methoxy-2-(4-methoxyphenoxy)

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:1655-72-7 SDS

1655-72-7Relevant articles and documents

Ullmann diaryl ether synthesis: rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione.

Buck, Elizabeth,Song, Zhiguo Jake,Tschaen, David,Dormer, Peter G,Volante,Reider, Paul J

, p. 1623 - 1626 (2002)

[reaction: see text]. In the copper salt catalyzed ether formation from aryl bromides or iodides and phenols, 2,2,6,6-tetramethylheptane-3,5-dione (TMHD) was found to greatly accelerate the ordinarily difficult reaction, making it occur under more moderate temperatures and reaction times. A series of aryl halides and phenols were shown to form ethers in NMP as the solvent, cesium carbonate as the base, and CuCl and TMHD as the catalysts. The reaction was shown to tolerate electron-rich aryl bromides and electron-neutral phenols.

Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine

Evans, David A.,Katz, Jeffrey L.,West, Theodore R.

, p. 2937 - 2940 (2007/10/03)

Diaryl ethers are readily synthesized in high yield at room temperature through the copper(II)-promoted coupling of arylboronic acids and phenols. The reaction is tolerant of a wide range of substituents on both coupling partners. These reaction condition

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