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217797-14-3

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  • (3S,4R)-3-[(1,3-Benzodioxol-5-yloxy)methyl]-4-phenylpiperidine me thanesulfonate (1:1)

    Cas No: 217797-14-3

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217797-14-3 Usage

Uses

Different sources of media describe the Uses of 217797-14-3 differently. You can refer to the following data:
1. Treatment of major depressive disorder, obsessive compulsive disorder, and panic disorder (selective serotonin reuptake inhibitor).
2. Paroxetine Mesylate is a selective serotonin reuptake inhibitor in treatment of depression in human, dog, cat, horse and parrot.

Brand name

Pexeva (JDS).

Check Digit Verification of cas no

The CAS Registry Mumber 217797-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,7,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 217797-14:
(8*2)+(7*1)+(6*7)+(5*7)+(4*9)+(3*7)+(2*1)+(1*4)=163
163 % 10 = 3
So 217797-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NO3.CH4O3S/c1-2-4-14(5-3-1)17-8-9-20-11-15(17)12-21-16-6-7-18-19(10-16)23-13-22-18;1-5(2,3)4/h1-7,10,15,17,20H,8-9,11-13H2;1H3,(H,2,3,4)/t15-,17-;/m0./s1

217797-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Paroxetine mesylate

1.2 Other means of identification

Product number -
Other names Paroxetine methanesulfonate

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:217797-14-3 SDS

217797-14-3Synthetic route

(3S,4R)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine-1-carboxylic acid phenyl ester
253768-88-6

(3S,4R)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine-1-carboxylic acid phenyl ester

paroxetine mesylate
217797-14-3

paroxetine mesylate

Conditions
ConditionsYield
With potassium hydroxide; methanesulfonic acid In toluene

217797-14-3Downstream Products

217797-14-3Relevant articles and documents

Process for the production of paroxetine

-

, (2008/06/13)

The synthesis of paroxetine can be made more convenient by using a solvent system comprising an aliphatic alcohol and a hydrocarbon co-solvent. The solvent system is used particularly in the hydrolysis of paroxetine phenylcarbamate and preferably uses butanol and toluene as the system.

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