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(1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-amine is a complex organic compound with a molecular formula of C16H15Cl2N. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of compounds known as tetrahydronaphthalenes. This specific compound features a naphthalene core, which is a fused ring system consisting of two benzene rings, with one of the rings being partially saturated to form a tetrahydro structure. The molecule also contains a 3,4-dichlorophenyl group attached to the 4-position of the tetrahydronaphthalene, which introduces two chlorine atoms at the 3 and 4 positions of the phenyl ring. The amine group is located at the 1-position, indicating the presence of a nitrogen atom with one hydrogen atom and one substituent attached to it. (1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-amine is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a precursor in the synthesis of other complex molecules.

87857-41-8

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87857-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87857-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87857-41:
(7*8)+(6*7)+(5*8)+(4*5)+(3*7)+(2*4)+(1*1)=188
188 % 10 = 8
So 87857-41-8 is a valid CAS Registry Number.

87857-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Norsertraline

1.2 Other means of identification

Product number -
Other names (1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-amine

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:87857-41-8 SDS

87857-41-8Relevant academic research and scientific papers

An expedient total synthesis of cis-(+)-sertraline from D-phenylglycine

Chandrasekhar,Venkat Reddy

, p. 1111 - 1114 (2007/10/03)

An efficient and practical total synthesis of cis-(+)-Sertraline is developed involving intramolecular Friedel-Crafts cyclization of an appropriately tailored D-phenylglycine. (C) 2000 Elsevier Science Ltd.

Selective functionalization of 1,2-dihydronaphthalenols leads to a concise, stereoselective synthesis of sertraline

Lautens, Mark,Rovis, Tomislav

, p. 8967 - 8976 (2007/10/03)

Asymmetric reductive ring opening of oxabenzonorbornadiene provides dihydronaphthalenols in high ee and good yield. Functionality present in this system can be used to elaborate the core towards a number of targets. As an illustration, a concise stereoselective synthesis of the important antidepressant sertraline is described.

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