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(1S,4R) Sertraline Hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79896-31-4

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79896-31-4 Usage

Chemical Properties

White Solid

Uses

Enantiomer 1S,4R of Sertraline. Antidepressant

Check Digit Verification of cas no

The CAS Registry Mumber 79896-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,9 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79896-31:
(7*7)+(6*9)+(5*8)+(4*9)+(3*6)+(2*3)+(1*1)=204
204 % 10 = 4
So 79896-31-4 is a valid CAS Registry Number.

79896-31-4SDS

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 (1S,4R)-4-(3,4-dichlorophenyl)-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names (1S,4R) Sertraline Hydrochloride

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:79896-31-4 SDS

79896-31-4Downstream Products

79896-31-4Relevant academic research and scientific papers

Concise enantioselective synthesis of (+)-sertraline and (-)-CP-52002 using proline catalysis

Kalshetti, Rupali,Venkataramasubramanian,Kamble, Sanjay,Sudalai, Arumugam

, p. 1053 - 1055 (2016/02/16)

A short enantioselective synthesis of (+)-sertraline and its C4 epimer (-)-CP-52002 with an overall yield of 30%, respectively, as its hydrochloride has been described. The key steps are the proline catalyzed Mannich reaction of acetaldehyde and acid catalyzed intramolecular Friedel-Crafts' alkylation reaction of olefin proceeding with high optical purities.

COMBINATIONS OF ESZOPICLONE AND TRANS 4-(3,4-DICHLOROPHENYL)-1,2,3,4-TETRAHYDRO-N-METHYL-1-NAPTHALENAMINE OR TRANS 4-(3,4-DICHLOROPHENYL)-1,2,3,4-TETRAHYDRO-1-NAPTHALENAMINE, AND METHODS OF TREATMENT OF MENOPAUSE AND MOOD, ANXIETY, AND COGNITIVE DISORDERS

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Page/Page column 20; 24, (2008/06/13)

One aspect of the present invention relates to pharmaceutical compositions containing two or more active agents that when taken together can be used to treat, e.g., menopause, mood disorders, anxiety disorders, or cognitive disorders. The first component of the pharmaceutical composition is a sedative eszopiclone. The second component of the pharmaceutical composition is trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-napthalenamine or trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine. The present invention also relates to a method of treating menopause, perimenopause, mood disorders, anxiety disorders, and cognitive disorders.

PROCESSES FOR PREPARING SERTRALINE

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Page/Page column 20-21; 23-25, (2008/06/13)

Provided are processes for the preparation of sertraline and sertraline hydrochloride.

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