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[3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene, also known as bis(4-phenoxyphenyl)methane, is a chemical compound belonging to the class of phenoxy compounds. It is a white crystalline solid with a molecular formula of C41H38O4 and a molecular weight of 594.74 g/mol.

2209-94-1

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2209-94-1 Usage

Uses

Used in Organic Synthesis:
[3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for further chemical reactions and modifications, making it a valuable component in the development of new molecules with specific properties and applications.
Used in Materials Science:
In the field of materials science, [3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene may have potential applications due to its structural characteristics. Its properties could be harnessed to create new materials with specific characteristics, such as improved stability, strength, or other desirable traits.
Used in Pharmaceutical Research:
[3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene may also find use in pharmaceutical research, where its unique structure could be exploited to develop new drugs or drug candidates. Its potential interactions with biological systems and its ability to be modified through chemical reactions make it an interesting starting point for the development of novel therapeutic agents.
Used in Industrial and Commercial Applications:
While [3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene has potential industrial and commercial uses, it is essential to consider its proper handling and management. [3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene may pose environmental and health hazards, and therefore, it is crucial to follow safety protocols and regulations to minimize any potential risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 2209-94-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2209-94:
(6*2)+(5*2)+(4*0)+(3*9)+(2*9)+(1*4)=71
71 % 10 = 1
So 2209-94-1 is a valid CAS Registry Number.

2209-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-phenoxy-2,2-bis(phenoxymethyl)propoxy]benzene

1.2 Other means of identification

Product number -
Other names Tetrakis-phenoxymethyl-methan

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:2209-94-1 SDS

2209-94-1Relevant academic research and scientific papers

Organically doped palladium: A highly efficient catalyst for electroreduction of CO2 to methanol

Yang, Heng-Pan,Qin, Sen,Wang, Huan,Lu, Jia-Xing

, p. 5144 - 5148 (2015/12/05)

A [PYD]@Pd composite was prepared by the entrapment of a pyridine derivative within metallic palladium. Metallic Pd acts as a heterogeneous support and a pyridine ring served as an active site for electroreduction of CO2, and no additional catalyst was needed in the electrolyte. 35% Faradaic efficiency of methanol was obtained at only -0.6 V vs. SCE. Moreover, [PYD]@Pd has remarkable stability and reusability.

CuO nanoparticles catalyzed C-N, C-O, and C-S cross-coupling reactions: Scope and mechanism

Jammi, Suribabu,Sakthivel, Sekarpandi,Rout, Laxmidhar,Mukherjee, Tathagata,Mandai, Santu,Mitra, Raja,Saha, Prasenjit,Punniyamurthy, Tharmalingam

supporting information; scheme or table, p. 1971 - 1976 (2009/07/01)

CuO nanoparticles have been studied for C-N, C-O, and C-S bond formations via cross-coupling reactions of nitrogen, oxygen, and sulfur nucleophiles with aryl halides. Amides, amines, imidazoles, phenols, alcohols and thiols undergo reactions with aryl iodides in the presence of a base such as KOH, Cs 2CO3, and K2CO3 at moderate temperature. The procedure is simple, general, ligand-free, and efficient to afford the cross-coupled products in high yield.

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