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54757-44-7

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  • High quality [5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide supplier in China

    Cas No: 54757-44-7

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54757-44-7 Usage

Description

[5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide is a complex organic compound with a unique molecular structure. It is characterized by its triphenylphosphonium cation and a pentadienyl anion with a substituted phenyl group. [5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide is known for its potential applications in various fields, particularly as a research chemical.

Uses

Used in Research Applications:
[5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide is used as a research chemical for exploring its properties and potential applications in various scientific fields. Its unique structure and reactivity make it a valuable compound for studying chemical reactions and mechanisms.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide may be utilized as a starting material or intermediate in the synthesis of novel drugs or drug candidates. Its specific properties and reactivity could be harnessed to develop new therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Chemical Synthesis:
[5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide can also be used in chemical synthesis as a reagent or catalyst to facilitate specific reactions. Its unique structure may enable it to act as a catalyst in certain chemical processes, potentially increasing the efficiency and selectivity of these reactions.
Used in Material Science:
In the field of material science, [5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadien-1-yl]triphenylphosphonium bromide may be investigated for its potential use in the development of new materials with specific properties. Its unique molecular structure could contribute to the creation of materials with enhanced characteristics, such as improved conductivity, stability, or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 54757-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,5 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54757-44:
(7*5)+(6*4)+(5*7)+(4*5)+(3*7)+(2*4)+(1*4)=147
147 % 10 = 7
So 54757-44-7 is a valid CAS Registry Number.

54757-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienyl]-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names (5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dien-1-yl)triphenylphosphonium bromide

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:54757-44-7 SDS

54757-44-7Relevant articles and documents

PROCESS FOR PREPARATION OF ACITRETIN

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, (2016/04/20)

The present invention provides a process for preparation of {(2E,4E,6E,8E)-9-(4-methoxy-2,3,6- trimethyl)phenyl-3,7-dimethyl-nona-2,4,6,8}tetraenoate, an acitretin intermediate of formula (VI) with trans isomer ≥97%, comprising of reacting 3-formyl-crotonic acid butyl ester of formula (V), substantially free of impurities, with 5-(4-methoxy-2,3,6-trimethylphenyl)-3- methyl-penta-2,4-diene-l-triphenyl phosphonium bromide of formula (IV) and isolating resultant compound of formula (VI), treating the filtrate with iodine for isomerization of the undesired cis intermediate and finally obtaining acitretin (I), with desired trans isomer ≥97%.

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