Pyridinium, 2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-,4-methylbenzenesulfonate (1:1)

Base Information

Chemical Name:Pyridinium, 2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-,4-methylbenzenesulfonate (1:1)
CAS No.:7596-85-2
Molecular Formula:C₇H₇O₃S*C₂₄H₂₄NO₂
Molecular Weight:529.657
Hs Code.:

Synonyms:Pyridinium, 2,6-bis(p-methoxystyryl)-1-methyl-,p-toluenesulfonate (5CI); Pyridinium,2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-, saltwith 4-methylbenzenesulfonic acid (1:1) (9CI); NSC 34618

Suppliers and Price of Pyridinium, 2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-,4-methylbenzenesulfonate (1:1)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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Total 2 raw suppliers

Chemical Property of Pyridinium, 2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-,4-methylbenzenesulfonate (1:1)

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Pyridinium, 2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-,4-methylbenzenesulfonate (1:1)

There total 2 articles about Pyridinium, 2,6-bis[2-(4-methoxyphenyl)ethenyl]-1-methyl-,4-methylbenzenesulfonate (1:1) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 7596-85-2
2,6-bis-(4-methoxy-trans-styryl)-1-methyl-pyridinium; toluene-4-sulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid anhydride

2: 160 - 180 °C

With acetic anhydride;
DOI:10.1021/jo01188a007