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Sultopride

Product Name
Sultopride
CAS No.
53583-79-2
Chemical Name
Sultopride
Synonyms
LIN 1418;Barnetil;Sultopride;Sultopridum;N-[(1-Ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxybenzamide;Benzamide, N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxy-;N-[(1-Ethylpyrrolidin-2-yl)methyl]-5-(ethylsulfonyl)-2-(methyloxy)benzamide;4-amino-N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxybenzamid;Benzamide, N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxy- (9CI)
CBNumber
CB2875390
Molecular Formula
C17H26N2O4S
Formula Weight
354.468
MOL File
53583-79-2.mol
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Sultopride Property

Melting point:
181-182 °C
Boiling point:
530.0±50.0 °C(Predicted)
Density 
1.1814 (rough estimate)
refractive index 
1.6930 (estimate)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
13.99±0.46(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0001590
Product name
BARNETIL
Purity
95.00%
Packaging
5MG
Price
$500.01
Updated
2021/12/16
CSNpharm
Product number
CSN21847
Product name
Sultopride
Packaging
50mg
Price
$595
Updated
2021/12/16
CSNpharm
Product number
CSN21847
Product name
Sultopride
Packaging
5mg
Price
$102
Updated
2021/12/16
CSNpharm
Product number
CSN21847
Product name
Sultopride
Packaging
10mg
Price
$179
Updated
2021/12/16
CSNpharm
Product number
CSN21847
Product name
Sultopride
Packaging
25mg
Price
$357
Updated
2021/12/16
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Sultopride Chemical Properties,Usage,Production

Originator

Barnetil,Delagrange,France,1976

Definition

ChEBI: Sultopride is a member of salicylamides.

Manufacturing Process

A solution of 17.22 g of N-ethyl-α-aminomethylpyrrolidine in 360 ml of pyridine is placed in a 1 l balloon flask. A solution of 3.51 g of phosphorus trichloride in 40 ml of pyridine is added at ambient temperature. After the mixture has been stirred for 1 hour, 10 g of 2-methoxy-5-ethylsulfonylbenzoic acid is introduced. The mixture is heated under reflux for 4 ? hours. After cooling, the solvent is evaporated under vacuum and the residue is dissolved in 200 ml of 20% sodium hydroxide. The solution is extracted with 200 ml of chloroform.
The organic solution is dried and filtered and the solvent is evaporated under vacuum; the residue is dissolved in 150 ml of ethanol and the solution is acidified with hydrochloric acid. The hydrochloride is dried without heating and recrystallized from 100 ml of absolute ethanol. 7.2 g of N-(1-ethyl-2- pyrrolidyl-methyl-2-methoxy-5-ethylsulfonylbenzamide hydrochloride is produced. Melting point: 190°C to 193°C.

brand name

Banotil;Barnotil;Topral.

Therapeutic Function

Neuroleptic

Sultopride Preparation Products And Raw materials

Raw materials

Preparation Products

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Sultopride Suppliers

Hangzhou Yuhao Chemical Technology Co., Ltd
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53583-79-2, SultoprideRelated Search:


  • Sultopride
  • Barnetil
  • Benzamide, N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxy- (9CI)
  • LIN 1418
  • N-[(1-Ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxybenzamide
  • N-[(1-Ethylpyrrolidin-2-yl)methyl]-5-(ethylsulfonyl)-2-(methyloxy)benzamide
  • Benzamide, N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxy-
  • Sultopridum
  • 4-amino-N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxybenzamid
  • 53583-79-2