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(R)-1-(3-METHOXYPHENYL)ETHYLAMINE-HCl is a chemical compound that features a substituted phenethylamine group and a chloride ion. It is the salt form of (R)-1-(3-Methoxyphenyl)ethylamine, an organic compound with potential applications in pharmaceutical research and development, as well as in neuroscience. The HCl salt form enhances the stability and solubility of the compound, making it suitable for a range of experimental and analytical uses.

1167414-89-2

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1167414-89-2 Usage

Uses

Used in Pharmaceutical Research and Development:
(R)-1-(3-METHOXYPHENYL)ETHYLAMINE-HCl is used as a precursor in the synthesis of various bioactive compounds, contributing to the development of new pharmaceuticals.
Used in Neuroscience:
(R)-1-(3-METHOXYPHENYL)ETHYLAMINE-HCl is used as a research compound in the field of neuroscience, potentially aiding in the study of neurological processes and the development of treatments for related conditions.
Used as a Reference Standard for Chromatography:
(R)-1-(3-METHOXYPHENYL)ETHYLAMINE-HCl is utilized as a reference standard in chromatographic techniques, ensuring accurate analysis and identification of compounds in experimental and analytical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1167414-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,7,4,1 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1167414-89:
(9*1)+(8*1)+(7*6)+(6*7)+(5*4)+(4*1)+(3*4)+(2*8)+(1*9)=162
162 % 10 = 2
So 1167414-89-2 is a valid CAS Registry Number.

1167414-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-(3-Methoxyphenyl)ethanamine hydrochloride

1.2 Other means of identification

Product number -
Other names (1R)-1-(3-methoxyphenyl)ethanamine,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:1167414-89-2 SDS

1167414-89-2Relevant academic research and scientific papers

General strategy for large-scale synthesis of (+)-rivastigmine and (+)-NPS R-568

Rao, Ramakrishna,Shewalkar, Mukesh Padmakar,Nandipati, Ramadevi,Yadav, Jhillu Singh,Khagga, Mukkanti,Shinde, Devanand Baburao

, p. 589 - 598 (2011/11/29)

An economically viable strategy for the total synthesis of (+)-rivastigmine and (+)-NPS R-568 has been reported. The strategy involves regioselective hydrogenation of diastereomerically pure bis amine to realize the desired a-methyl chiral substituted benzyl amine. The route is economical, scalable, and versatile enough to be adapted to similar classes of compounds. Taylor & Francis Group, LLC.

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