1-(2-carboxyethyl)-4-pyridinium betaine

Base Information

Chemical Name:1-(2-carboxyethyl)-4-pyridinium betaine
CAS No.:90133-95-2
Molecular Formula:C₂₄H₃₂N₂O₂
Molecular Weight:380.53
Hs Code.:

1-(2-carboxyethyl)-4-<p-(di-n-butylamino)styryl>pyridinium betaine

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Suppliers and Price of 1-(2-carboxyethyl)-4-pyridinium betaine

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

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Chemical Property of 1-(2-carboxyethyl)-4-pyridinium betaine

Chemical Property:

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Technology Process of 1-(2-carboxyethyl)-4-pyridinium betaine

There total 4 articles about 1-(2-carboxyethyl)-4-pyridinium betaine 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: 48.0%

: 90133-94-1
trans-4-pyridine

: 43165-24-8
sodium salt of bromopropionic acid

: 90133-95-2,97807-62-0
1-(2-carboxyethyl)-4-pyridinium betaine

Guidance literature:: In ethanol; for 16h; Heating;
DOI:10.1021/jo00188a006

Reference yield:

: 100-43-6,329041-72-7
4-vinylpyridine

: 90133-95-2,97807-62-0
1-(2-carboxyethyl)-4-pyridinium betaine

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / tri-o-tolylphsphine / palladium diacetate / triethylamine / 72 h / 110 °C

With tris-(o-tolyl)phosphine; palladium diacetate; In triethylamine;
DOI:10.1021/jo00188a006

Reference yield:

: 53358-54-6
1-bromo-4-(N,N-dibutyl)aniline

: 90133-95-2,97807-62-0
1-(2-carboxyethyl)-4-pyridinium betaine

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / tri-o-tolylphsphine / palladium diacetate / triethylamine / 72 h / 110 °C

With tris-(o-tolyl)phosphine; palladium diacetate; In triethylamine;
DOI:10.1021/jo00188a006