Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-(4-methoxyphenoxy)-3-methylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82721-04-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 82721-04-8 Structure
  • Basic information

    1. Product Name: 1-(4-methoxyphenoxy)-3-methylbenzene
    2. Synonyms:
    3. CAS NO:82721-04-8
    4. Molecular Formula: C14H14O2
    5. Molecular Weight: 214.2598
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82721-04-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 311.1°C at 760 mmHg
    3. Flash Point: 120.7°C
    4. Appearance: N/A
    5. Density: 1.069g/cm3
    6. Vapor Pressure: 0.00105mmHg at 25°C
    7. Refractive Index: 1.554
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(4-methoxyphenoxy)-3-methylbenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(4-methoxyphenoxy)-3-methylbenzene(82721-04-8)
    12. EPA Substance Registry System: 1-(4-methoxyphenoxy)-3-methylbenzene(82721-04-8)
  • 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: 82721-04-8(Hazardous Substances Data)

82721-04-8 Usage

Chemical classes

Aromatic ether, alkylbenzene

Industrial applications

a. Solvent
b. Intermediate
c. Production of synthetic flavors and fragrances

Safety precautions

a. Potential skin irritation
b. Potential eye irritation
c. Potential respiratory system irritation

Handling

Use caution to avoid contact with skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 82721-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,2 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82721-04:
(7*8)+(6*2)+(5*7)+(4*2)+(3*1)+(2*0)+(1*4)=118
118 % 10 = 8
So 82721-04-8 is a valid CAS Registry Number.

82721-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-(3-methylphenoxy)benzene

1.2 Other means of identification

Product number -
Other names 1-methoxy-4-m-tolyloxybenzene

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:82721-04-8 SDS

82721-04-8Relevant articles and documents

Aromatic ether compound or the sulfhydryl compound

-

Paragraph 0083-0084; 0099-0100; 0109, (2021/11/19)

[Problem] Aromatic ether compounds and aromatic sulfide compound of this new technology to[Solution] In general formula (1a), (1b), (1c) palladium or nickel compound or a phosphine compound represented by the compound comprising a transition metal compound in the presence of a transition metal catalyst, (A1) is represented by compounds having hydroxy carbon C a-OH or (A2) with a compound represented by the sulfhydryl carbon C a-SH, nitro group (- NO2 ) To react with an aromatic nitro compound (B), (A1) to the compound of the aromatic nitro compound (C1) or the reaction product of an aromatic ether compounds (B) hetero coupling (A2) of the compounds of the reaction product of an aromatic sulfide compound of an aromatic nitro compound (C2) generating (B) hetero coupling characterized by comprising the step of, aromatic ether compounds or aromatic sulfide compound. [Drawing] no

Pd-Catalyzed Etherification of Nitroarenes

Matsushita, Naoki,Kashihara, Myuto,Formica, Michele,Nakao, Yoshiaki

supporting information, p. 2209 - 2214 (2021/07/20)

The Pd-catalyzed etherification of nitroarenes with arenols has been achieved using a new rationally designed ligand. Mechanistic insights were used to design the ligand so that both the oxidative addition and reductive elimination steps of a plausible catalytic cycle were facilitated. The catalytic system established here provides direct access to a range of unsymmetrical diaryl ethers from nitroarenes.

Magnetically recyclable nano copper/chitosan in O-arylation of phenols with aryl halides

Mousavi Mashhadi, Seyed Ali,Kassaee, Mohamad Z.,Eidi, Esmaiel

, (2019/07/04)

Interaction of chitosan (CS) with Fe3O4, followed by embedding Cu nanoparticles (NPs) on the magnetic surface through adsorption of Cu2+, and its reduction to Cuo via NaBH4, offers a reusable efficient catalyst (Fe3O4/CS-Cu NPs) that is employed in cross-coupling reactions of aryl halides with phenols, which affords the corresponding diaryl ethers, with good to excellent yields. The catalyst is completely recoverable from the reaction mixture by using an external magnet. It can be reused four times, without significant loss in its catalytic activity.

Low catalyst loadings for copper-catalyzed O-arylation of phenols with aryl and heteroaryl halides under mild conditions

Yong, Fui-Fong,Teo, Yong-Chua,Yan, Yaw-Kai,Chua, Guan-Leong

scheme or table, p. 101 - 106 (2012/02/03)

A practical and mild strategy has been developed for the cross-coupling of O-arylation of phenol with differently substituted aryl halides and heteroaryl iodides using low catalyst loading of copper iodide under low operating temperature in DMF with TMHD as the ligand and Cs2CO3 as the base. This method tolerates a variety of functional groups including sterically hindered phenols and heteroaryl iodides to afford products in good to excellent yields (up to 95%). Georg Thieme Verlag Stuttgart. New York.

1,1,1-Tris(hydroxymethyl)ethane as a new, efficient, and versatile tripod ligand for copper-catalyzed cross-coupling reactions of aryl iodides with amides, thiols, and phenols

Chen, Yao-Jung,Chen, Hsin-Hung

, p. 5609 - 5612 (2007/10/03)

1,1,1-Tris(hydroxymethyl)ethane was presented as a new, efficient, and versatile tridentate O-donor ligand suitable for the copper-catalyzed formation of C-N, C-S, and C-O bonds. This inexpensive and commercially available tripod ligand has been demonstrated to facilitate the copper-catalyzed cross-coupling reactions of aryl iodides with amides, thiols, and phenols to afford the corresponding desired products in good to excellent yields.

N,N-Dimethyl Glycine-Promoted Ullmann Coupling Reaction of Phenols and Aryl Halides

Ma, Dawei,Cai, Qian

, p. 3799 - 3802 (2007/10/03)

(Matrix presented) Ullmann-type diaryl ether synthesis can be performed at 90°C using either aryl iodides or aryl bromides as the substrates under the assistance of N,N-dimethylglycine.

Carbamic acid esters

-

, (2008/06/13)

Carbamic acid esters of the formula STR1 wherein R1, R2, R3, R4, R5, R6, R7, X, and Y are as defined hereinafter, process for their preparation, as well as pesticidal compositions containing these compounds as the active ingredient and methods for using the pesticidal compositions for the control of pests are described.

Carbamic acid esters and use as pesticides

-

, (2008/06/13)

Carbamic acid compounds of the formula STR1 wherein R1, R2, R3, R4, R5, R6, X and Y are as hereinafter set forth, processes for their preparation, pesticidal compositions containing one or more of the carbamic acid compounds as the active ingredient and methods for using the pesticidal compositions for the control of pests, particularly insects, mites and nematodes, are described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 82721-04-8