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39170-14-4

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39170-14-4 Usage

General Description

5-(4-Chlorophenyl)-2-furyl) methylamine, also known as E-682, is a novel psychoactive substance that acts as a selective serotonin releasing agent and a norepinephrine releasing agent. It is structurally related to phenethylamine and shares similarities with the drug MDMA, though its effects are reported to be longer-lasting. E-682 has been studied as a potential treatment for depression and anxiety, as well as for its potential as a recreational drug. However, due to its psychoactive effects and potential for abuse, it is classified as a controlled substance in many countries. Research into its safety, efficacy, and potential for harm is ongoing.

Check Digit Verification of cas no

The CAS Registry Mumber 39170-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39170-14:
(7*3)+(6*9)+(5*1)+(4*7)+(3*0)+(2*1)+(1*4)=114
114 % 10 = 4
So 39170-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClNO/c12-9-3-1-8(2-4-9)11-6-5-10(7-13)14-11/h1-6H,7,13H2/p+1

39170-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(4-CHLOROPHENYL)-2-FURYL]METHYLAMINE

1.2 Other means of identification

Product number -
Other names -

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:39170-14-4 SDS

39170-14-4Relevant articles and documents

Aryl Radical Selectivity in Biphasic Systems

Altmann, Lisa-Marie,Fürst, Michael C. D.,Gans, Eva I.,Heinrich, Markus R.,Pratsch, Gerald,Zantop, Viviane

supporting information, (2020/01/31)

Aryl radicals generated in the aqueous phase of biphasic mixtures have-regardless of a comparably low polarity- A strong preference to react with aromatic substrates in the aqueous phase and not to undergo phase-transfer into a lipophilic phase, independent from the presence of a surfactant. These results represent an important prerequisite toward future studies in biological systems, which typically consist of various compartments of either hydrophilic or lipophilic character.

Visible-Light-Induced, Catalyst-Free Radical Arylations of Arenes and Heteroarenes with Aryldiazonium Salts

Fürst, Michael C. D.,Gans, Eva,B?ck, Michael J.,Heinrich, Markus R.

supporting information, p. 15312 - 15315 (2017/10/20)

In the absence of a photocatalyst and other additives, the radical arylation of diverse arenes and heteroarenes has been achieved with aryldiazonium salts under visible-light irradiation from a blue light-emitting diode (LED). Although the course of some reactions can be rationalized by the formation of strongly light-absorbing charge-transfer (CT) complexes between the diazonium ion and the aromatic substrate, several further examples indicated that the simple presence of an aromatic substrate, showing only weak interactions to the diazonium ion, is fully sufficient to enable product formation.

Radical arylation of phenols, phenyl ethers, and furans

Wetzel, Alexander,Pratsch, Gerald,Kolb, Roman,Heinrich, Markus R.

experimental part, p. 2547 - 2556 (2010/06/17)

Radical arylations of parasubstituted phenols and phenyl ethers proceeded with good regioselectivity at the ortho position with respect to the hydroxy or alkoxy group. The reactions were conducted with arenediazonium salts as the aryl radical source, titaniumACHTUNGTRENUNG(III) chloride as the reductant, and diluted hydrochloric acid as the solvent. Substituted biaryls were obtained from hydroxy- and alkoxy-substituted benzylamines, phenethylamines, and aromatic amino acids. The methodology described offers a fast, efficient, and cost-effective new access todiversely functionalized biphenyl alcohols and ethers. Free phenolic hydroxyl groups, aromatic and aliphatic amines, as well as amino acid substructures, are well tolerated. Two examples for the applicability of the methodology are the partial synthesis of a b-secretase inhibitor and the synthesis of a calciumchannel modulator

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