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456-05-3

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456-05-3 Usage

General Description

α-(Aminomethyl)-4-fluorobenzyl alcohol, also known as 4-F-amphetamine, is a chemical compound that acts as a central nervous system stimulant and a substrate for the vesicular monoamine transporter. It is used as a research chemical and has been studied for its potential use as a psychotherapeutic medication. As a derivative of amphetamine, it is structurally related to other psychoactive substances such as methamphetamine and MDMA. It exhibits neurotoxicity and can potentially have negative effects on the cardiovascular system, and as such, its use and distribution are heavily regulated in many jurisdictions. Research on this compound continues in order to better understand its pharmacological effects and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 456-05-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 456-05:
(5*4)+(4*5)+(3*6)+(2*0)+(1*5)=63
63 % 10 = 3
So 456-05-3 is a valid CAS Registry Number.

456-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(4-fluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(4-fluor-phenyl)-aethanol

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:456-05-3 SDS

456-05-3Relevant articles and documents

DOPAMINE D3 RECEPTOR ANTAGONISTS HAVING A MORPHOLINE MOIETY

-

, (2018/11/21)

The disclosure provides compounds of formula (I) or pharmaceutically acceptable salts thereof: The disclosure also provides processes for their preparation, intermediates used in these processes, pharmaceutical compositions containing them, and their use

Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitors

Liu, Feng,Li, Fengling,Ma, Anqi,Dobrovetsky, Elena,Dong, Aiping,Gao, Cen,Korboukh, Ilia,Liu, Jing,Smil, David,Brown, Peter J.,Frye, Stephen V.,Arrowsmith, Cheryl H.,Schapira, Matthieu,Vedadi, Masoud,Jin, Jian

, p. 2110 - 2124 (2013/05/08)

Protein arginine methyltransferases (PRMTs) play an important role in diverse biological processes. Among the nine known human PRMTs, PRMT3 has been implicated in ribosomal biosynthesis via asymmetric dimethylation of the 40S ribosomal protein S2 and in c

Efficient preparation of biologically important 1,2-amino alcohols

Gupta, Pankaj,Rouf, Abdul,Shah, Bhahwal A.,Mukherjee, Debaraj,Taneja, Subhash C.

, p. 505 - 519 (2013/01/15)

An efficient three-step methodology developed for the preparation of 1,2-amino alcohols. In the first step a rapid coupling between bromoketones and potassium phthalimide in ionic liquid produced-phthalimido ketones in quantitative yields, which is followed by a facile reduction using NaCNBH 3 in acetic acid to give corresponding phthalimido alcohols and finally effecting hydrazinolysis in water at 60C to yield biologically important 1,2-amino alcohols.

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