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2-(3-Fluoro-phenyl)-2-methyl-propylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160358-04-3

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160358-04-3 Usage

Chemical composition

Consists of a fluoro-phenyl group and a methyl-propylamine group.

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals.

Potential use

Treatment of neurological disorders.

Biological activities

Exhibits antiviral, anti-inflammatory, and neuroprotective properties.

Additional properties

Has potential as an antioxidant and as a modulator of neurotransmitter release.

Versatility

Has promising applications in the fields of medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 160358-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,3,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160358-04:
(8*1)+(7*6)+(6*0)+(5*3)+(4*5)+(3*8)+(2*0)+(1*4)=113
113 % 10 = 3
So 160358-04-3 is a valid CAS Registry Number.

160358-04-3SDS

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 2-(3-Fluoro-phenyl)-2-methyl-propylamine

1.2 Other means of identification

Product number -
Other names 2-(3-fluorophenyl)-2-hydroxyethanamine

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:160358-04-3 SDS

160358-04-3Relevant academic research and scientific papers

NOVEL COMPOUNDS

-

Page/Page column 108, (2011/08/22)

The present invention relates to new CGRP-antagonists of general formula I wherein U, V, X, Y, R1, R2, R3 and R4 are defined as mentioned in the description, the tautomers thereof, the isomers thereof, the diastereomers thereof, the enantiomers thereof, the hydrates thereof, the mixtures thereof and the salts thereof as well as the hydrates of the salts, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, medicaments containing these compounds, the use thereof and processes for the preparation thereof.

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