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81347-68-4

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81347-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81347-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,4 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81347-68:
(7*8)+(6*1)+(5*3)+(4*4)+(3*7)+(2*6)+(1*8)=134
134 % 10 = 4
So 81347-68-4 is a valid CAS Registry Number.

81347-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chloro-1-phenylpropoxy)-4-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 3-phenyl-3-(o-methylphenoxy)propylamine 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:81347-68-4 SDS

81347-68-4Relevant articles and documents

Dual Cobalt and Photoredox Catalysis Enabled Intermolecular Oxidative Hydrofunctionalization

Sun, Han-Li,Wang, Jun-Jie,Yang, Fan,Ye, Wei-Ting,Zhu, Rong

, p. 4983 - 4989 (2020/05/27)

A general protocol has been developed for the Markovnikov-selective intermolecular hydrofunctionalization based on visible-light-mediated Co/Ru dual catalysis. The key feature involves the photochemical oxidation of an organocobalt(III) intermediate deriv

MODULATORS OF CENTRAL NERVOUS SYSTEM NEUROTRANSMITTERS

-

Page/Page column 147-148, (2010/10/20)

Disclosed are agents having pharmacological activity against cellular receptors and intracellular singaling, particularly receptors and sigaling pathways of central nervous system (CNS) neurotransmitters. Also disclosed are related methods and compositions for the treatment or prevention of diseases or disorders using the agents.

Identification and comparison of impurities in fluoxetine hydrochloride synthesized by seven different routes

Wirth, David D.,Miller, Marybeth S.,Boini, Sathish K.,Koenig, Thomas M.

, p. 513 - 519 (2013/08/07)

Fluoxetine HCl was prepared by seven different synthetic routes, all previously reported. The major impurities in each route were identified by GC/MS, HPLCMS, and gradient HPLC analysis. Impurities were classified as being derived from impurities in 4-chlorobenzotrifluoride, those arising during the SNAr reaction of this compound and 3-methylamino-1-phenyl-propanol, and those arising during the synthesis of this alcohol. Fifteen impurities belonging to the latter two categories were identified, and their structures were confirmed by synthesis of authentic material for most of the compounds. It was found that a variety of analytical tools was needed for complete characterization of the impurity profile of fluoxetine HCl and that purification of the intermediate and recrystallization of the drug itself are highly effective in minimizing the levels of the impurities.

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