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2,3,4,4'-tetramethoxy-1,1'-biphenyl is a chemical compound belonging to the class of aromatic hydrocarbons known as biphenyls. It is characterized by its molecular formula C16H18O4 and features four methoxy (CH3O) groups attached to the biphenyl core. 2,3,4,4'-tetramethoxy-1,1'-biphenyl's unique chemical structure and properties make it a promising candidate for various technological and industrial applications.

6271-59-6

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6271-59-6 Usage

Uses

Used in Organic Synthesis:
2,3,4,4'-tetramethoxy-1,1'-biphenyl is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its versatile structure allows for the synthesis of a wide range of organic molecules, making it valuable in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Materials Science:
In the field of materials science, 2,3,4,4'-tetramethoxy-1,1'-biphenyl has potential applications in the development of liquid crystal display (LCD) materials. Its unique molecular structure and properties may contribute to the creation of advanced materials with improved performance characteristics, such as enhanced stability, response time, and contrast ratios in LCD devices.
Used in Pharmaceutical Industry:
2,3,4,4'-tetramethoxy-1,1'-biphenyl is used as a building block in the synthesis of pharmaceutical compounds. Its chemical structure can be modified to create new drug candidates with potential therapeutic applications. Researchers can explore its use in the development of novel drugs for various medical conditions, leveraging its unique properties to enhance drug efficacy and safety.
Used in Agrochemical Industry:
In the agrochemical industry, 2,3,4,4'-tetramethoxy-1,1'-biphenyl can be utilized as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical versatility allows for the development of new compounds with improved efficacy, selectivity, and environmental compatibility.
It is important to handle and use 2,3,4,4'-tetramethoxy-1,1'-biphenyl with caution, following proper safety protocols and guidelines to ensure the safety of both individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 6271-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6271-59:
(6*6)+(5*2)+(4*7)+(3*1)+(2*5)+(1*9)=96
96 % 10 = 6
So 6271-59-6 is a valid CAS Registry Number.

6271-59-6SDS

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 1,2,3-trimethoxy-4-(4-methoxyphenyl)benzene

1.2 Other means of identification

Product number -
Other names 2,3,4,4'-Tetramethoxy-1,1'-biphenyl

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:6271-59-6 SDS

6271-59-6Downstream Products

6271-59-6Relevant academic research and scientific papers

Structure-activity relationships of phenylcyclohexene and biphenyl antitubulin compounds against plant and mammalian cells

Young, David H.,Tice, Colin M.,Michelotti, Enrique L.,Roemmele, Renee C.,Slawecki, Richard A.,Rubio, Fernando M.,Rolling, Judith A.

, p. 1393 - 1396 (2007/10/03)

Phenylcyclohexenes (PCHs) [e.g., trans-4-nitro-5-(2,3,4-trimethoxyphenyl)cyclohexene, 2d] were found to bind weakly to the colchicine site of bovine tubulin, but are the first mimics of colchicine found to have high activity towards plant cells. Structure

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