Welcome to LookChem.com Sign In|Join Free
  • or
Benzenepropanamine, N-ethyl-N-phenyl-, also known as N-ethyl-N-phenylpropan-1-amine or N-ethyl-N-phenyl-1-phenylpropanamine, is an organic compound with the chemical formula C15H21N. It is a derivative of benzenepropanamine, featuring an ethyl group and a phenyl group attached to the nitrogen atom. Benzenepropanamine, N-ethyl-N-phenyl- is a colorless to pale yellow liquid with a characteristic amine-like odor. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its amine functional group, it can undergo a range of chemical reactions, such as acylation, alkylation, and substitution, making it a versatile building block in organic chemistry.

71982-21-3

Post Buying Request

71982-21-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

71982-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71982-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71982-21:
(7*7)+(6*1)+(5*9)+(4*8)+(3*2)+(2*2)+(1*1)=143
143 % 10 = 3
So 71982-21-3 is a valid CAS Registry Number.

71982-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-(3-phenylpropyl)aniline

1.2 Other means of identification

Product number -
Other names N-ethyl-N-(3-phenyl-propyl)-aniline

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:71982-21-3 SDS

71982-21-3Downstream Products

71982-21-3Relevant academic research and scientific papers

Carboxamides as N-Alkylating Reagents of Secondary Amines in Indium-Catalyzed Reductive Amination with a Hydrosilane

Ogiwara, Yohei,Shimoda, Wataru,Ide, Keisuke,Nakajima, Takumi,Sakai, Norio

supporting information, p. 2866 - 2870 (2017/06/06)

A method for the catalytic reductive N-alkylation of amines by using secondary amides as the alkyl source was developed. A versatile type of carboxamide functioned as an N-alkylation reagent in the presence of an indium(III) catalyst and a hydrosilane to provide alkylated tertiary amines efficiently. This amide-based catalytic N-alkylation strategy is considered to be a highly useful protocol to access unsymmetrical tertiary amines.

Iron-catalysed tandem isomerisation/hydrosilylation reaction of allylic alcohols with amines

Li, Haoquan,Achard, Mathieu,Bruneau, Christian,Sortais, Jean-Baptiste,Darcel, Christophe

, p. 25892 - 25897 (2014/07/07)

An iron(0)-catalysed cascade synthesis of N-alkylated anilines from allylic or homoallylic alcohols and primary and secondary anilines under hydrosilylation conditions has been developed. Notably, a simple Fe(cod)(CO)3 complex (cod = cycloocta-

Ruthenium-catalyzed reductive amination of allylic alcohols

Sahli, Zeyneb,Sundararaju, Basker,Achard, Mathieu,Bruneau, Christian

supporting information; experimental part, p. 3964 - 3967 (2011/09/21)

Straighforward access to various saturated amines from allylic alcohols and isostructural mixture can now be achieved in the presence of arene ruthenium catalyst featuring phosphinesulfonate ligand and a hydrogen donor.

One-pot synthesis of secondary and tertiary amines by carbonylative hydroaminomethylation of alkenes catalyzed by di(μ-chloro)bis(η4-1,5-cyclooctadiene)dirhodium

Rische,Eilbracht

, p. 1331 - 1337 (2007/10/03)

Secondary and tertiary amines are selectively prepared with high yields by the reaction of alkenes with primary or secondary amines, carbon monoxide and hydrogen in the presence of [Rh(cod)Cl]2 as catalyst via a one-pot hydroformylation - amine

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 71982-21-3