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N,N-Dipropylphenethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23916-02-1

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23916-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23916-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,1 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23916-02:
(7*2)+(6*3)+(5*9)+(4*1)+(3*6)+(2*0)+(1*2)=101
101 % 10 = 1
So 23916-02-1 is a valid CAS Registry Number.

23916-02-1SDS

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 N-(2-phenylethyl)-N-propylpropan-1-amine

1.2 Other means of identification

Product number -
Other names phenethyl-dipropyl-amine

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:23916-02-1 SDS

23916-02-1Relevant academic research and scientific papers

Hydroamination of terminal alkynes with secondary amines catalyzed by copper: Regioselective access to amines

Bahri, Janet,Blieck, Rémi,Jamoussi, Bassem,Taillefer, Marc,Monnier, Florian

supporting information, p. 11210 - 11212 (2015/07/07)

A simple and convenient copper-catalyzed hydroamination of arylacetylenes with secondary amines has been performed giving a simple access to aliphatic amines after reduction of the hydroaminated products (E-enamines). Here we described a mild catalytic system utilizing CuCN precatalyst without any additive ligands in a solvent-free system.

Borrowing hydrogen methodology for amine synthesis under solvent-free microwave conditions

Watson, Andrew J. A.,Maxwell, Aoife C.,Williams, Jonathan M. J.

supporting information; experimental part, p. 2328 - 2331 (2011/05/17)

Application of microwave heating to the Borrowing Hydrogen strategy to form C-N bonds from alcohols and amines is presented, removing the need for solvent and reducing the reaction times while still yielding results comparable with those using thermal heating.

Borrowing hydrogen in water and ionic liquids: Iridium-catalyzed alkylation of amines with alcohols

Saidi, Ourida,Blacker, A. John,Lamb, Gareth W.,Marsden, Stephen P.,Taylor, James E.,Williams, Jonathan M. J.

supporting information; experimental part, p. 1046 - 1049 (2011/03/20)

The use of [Cp*IrI2]2 as an efficient catalyst for the alkylation of amines by alcohols in either water or ionic liquid is described. Primary amines are converted into secondary amines, and secondary amines into tertiary amines in the absence of base, and the chemistry has been applied to the synthesis of the analgesic fentanyl. The conversion of primary amines into N-heterocycles by the reaction with diols is also described, along with the N-alkylation of sulfonamides.

D2 Dopaminergic and 5-HT1A Serotonergic Activity of 2-(1-Naphthyl)ethyl- and 2-(2-Naphthyl)ethyl Amines

?ukalovi?,Rogli?,Husinec,Kosti?-Raja?i?,Andri?,?o?ki?, Vuki?

, p. 514 - 522 (2007/10/03)

Several tertiary 2-phenylethyl, 2-(1-naphthyl)ethyl and 2-(2-naphthyl) ethyl amines were synthesized and their binding affinities for dopamine D 1, D2 and serotonin 5-HT1A receptors evaluated in radioligand binding assays.

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