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4,4'-Dimethoxy-2,2'5,5'-Tetraacetoxybiphenyl, commonly referred to as DMTAB, is a biphenyl compound characterized by the presence of four acetoxy groups on the phenyl rings and two methoxy groups at the 4 and 4' positions. This unique structure endows DMTAB with versatile applications in organic chemistry, particularly as a reagent for the selective oxidation of alcohols to carbonyl compounds. Its effectiveness and broad utility in the synthesis of various organic compounds make it a valuable asset in the field.

7461-72-5

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7461-72-5 Usage

Uses

Used in Organic Chemistry:
4,4'-Dimethoxy-2,2'5,5'-Tetraacetoxybiphenyl is used as a reagent for the selective oxidation of alcohols to carbonyl compounds, facilitating the synthesis of a wide range of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4,4'-Dimethoxy-2,2'5,5'-Tetraacetoxybiphenyl serves as a crucial building block for the synthesis of pharmaceutical intermediates, contributing to the development of new drugs and therapeutic agents.
Used in Materials Science:
4,4'-Dimethoxy-2,2'5,5'-Tetraacetoxybiphenyl is utilized in materials science for its potential applications in the creation of novel materials, leveraging its unique structural properties to enhance material performance.
Used in Medicinal Chemistry:
In medicinal chemistry, 4,4'-Dimethoxy-2,2'5,5'-Tetraacetoxybiphenyl is employed as a key component in the synthesis of various fine chemicals, which may have therapeutic or diagnostic applications.
Overall, the diverse applications of 4,4'-Dimethoxy-2,2'5,5'-Tetraacetoxybiphenyl across different industries highlight its significance as a versatile and valuable compound in modern scientific research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 7461-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7461-72:
(6*7)+(5*4)+(4*6)+(3*1)+(2*7)+(1*2)=105
105 % 10 = 5
So 7461-72-5 is a valid CAS Registry Number.

7461-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-acetyloxy-2-(2,5-diacetyloxy-4-methoxyphenyl)-5-methoxyphenyl] acetate

1.2 Other means of identification

Product number -
Other names (4,4'-Dimethoxy-biphenyltetrayl-(2,5,2',5'))-tetraacetat

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:7461-72-5 SDS

7461-72-5Relevant academic research and scientific papers

The Photochemical Discolouration of Methoxy-p-benzoquinone in Solution

Forsskahl, Ingegerg,Gustafsson, Jean,Nybergh, Anna

, p. 389 - 394 (2007/10/02)

Irradiation of a dimethoxyethane solution of methoxy-p-benzoquinone with sun-light lamps results in discolouration of the solution and the rapid disappearance of the starting material.A strongly coloured red dibenzofuran derivative, 8-hydroxy-3,7-dimethoxybenzofuran-1,4-quinone, was isolated from the reaction mixture and identified by comparison with the synthesized compound.The photochemical reactions of the possible intermediates, the dimer quinones 5-methoxy-2-(2,5-dihydroxy-4-methoxyphenyl)1,4-benzoquinone and 4,4'-dimethoxybiphenyl-2,5,2',5'-bis-quinone, were also studied by visible light spectroscopy and significant changes in the spectra were observed.It is concluded that these dimer quinones and their rearrangement products play a significant role in the production of colour in old methoxy-p-benzoquinone solutions and other solutions in which this quinone participates as an intermediate.In alkaline aqueous solution the isolated dibenzofuran derivative rapidly disappears via radical reactions.

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