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31904-34-4

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31904-34-4 Usage

General Description

(+/-)-N,N-Dimethyl-1-ferrocenylethylamine is a chemical compound with the molecular formula C15H18FeN. It is a ferrocene-based compound with a dimethylaminoethyl group attached to the ferrocenyl moiety. (+/-)-N,N-DIMETHYL-1-FERROCENYLETHYLAMINE is commonly used as a ligand in organometallic chemistry and catalysis, particularly in the synthesis of chiral metal complexes and asymmetric catalysis. Its unique structure and electronic properties make it useful in a variety of applications, including pharmaceuticals, materials science, and organic synthesis. It can also be used as a precursor for the synthesis of other ferrocene-based compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31904-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,0 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31904-34:
(7*3)+(6*1)+(5*9)+(4*0)+(3*4)+(2*3)+(1*4)=94
94 % 10 = 4
So 31904-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N.C5H4.Fe/c1-8(10(2)3)9-6-4-5-7-9;1-2-4-5-3-1;/h4-6,8H,1-3H3;1-4H;/q2*-1;+2/rC14H17FeN/c1-11(16(2)3)13-9-6-10-14(13)15-12-7-4-5-8-12/h4-11H,1-3H3

31904-34-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L19678)  (±)-N,N-Dimethyl-1-ferrocenylethylamine, 96%   

  • 31904-34-4

  • 1g

  • 584.0CNY

  • Detail
  • Alfa Aesar

  • (L19678)  (±)-N,N-Dimethyl-1-ferrocenylethylamine, 96%   

  • 31904-34-4

  • 5g

  • 2240.0CNY

  • Detail

31904-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-N,N-Dimethyl-1-ferrocenylethylamine

1.2 Other means of identification

Product number -
Other names (+/-)-N,N-DIMETHYL-1-FERROCENYLETHYLAMINE

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:31904-34-4 SDS

31904-34-4Relevant articles and documents

Synthetic method of Ugi's amines and derivatives of Ugi's amines

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Paragraph 0083-0092, (2019/05/16)

The invention discloses a synthetic method of Ugi's amines and derivatives of the Ugi's amines represented by a formula (I) shown in the description. The method comprises the following steps: performing reductive amination by using ferrocene and a derivative of the ferrocene as raw materials to obtain a racemic primary amine, performing resolution on the racemic primary amine by a resolving agentto obtain an optical isomer primary amine, performing an alkylation or reductive amination reaction on the optical isomer primary amine to obtain one Ugi's amine and the derivative of the Ugi's amine.The chiral Ugi's amines and the derivatives of the Ugi's amines provided by the invention can be used to synthesize a series of Josiphos-like ferrocene bisphosphine ligands, the Josiphos-like ferrocene bisphosphine ligands are used as chiral ligands for various metal complex catalysts, are important chiral catalyst ligands for preparation of pharmaceutical intermediates and agrochemicals, have awide range of applications in metal catalysis asymmetric reactions, and are suitable for industrialized large-scale production; and the reaction conditions are mild, the raw materials are cheap and easy to obtain, the synthetic route is simple, and the yield and chiral purity are higher.

Process for preparing (S)-1-ferrocene ethyl dimethylamine

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Paragraph 0050; 0053, (2018/09/11)

The invention discloses a process for preparing (S)-1-ferrocene ethyl dimethylamine. In the preparation process, acetylferrocene is used as a raw material, and a complex obtained by reacting a metal Ir complex with a chiral ferrocene tridentate ligand L* is used as a catalyst, (S)-1-ferrocenyl ethanol is prepared by asymmetric catalytic hydrogenation, and the(S)-1-ferrocene ethyl dimethylamine isprepared by acetylation and dimethylamine substitution reaction. Compared with a traditional chiral separation method for preparing the (S)-1-ferrocene ethyl dimethylamine, the process has main beneficial effects of mild reaction conditions, simple operation, good stereoselectivity, high yield, short production cycle, small amount of three wastes , easy industrialization, and large implementationvalue and social and economic benefits.

FUNCTIONALIZED MAGNETIC NANOPARTICLE, A CATALYST, A METHOD FOR FORMING C-C BONDS

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Paragraph 0194, (2018/04/20)

A functionalized magnetic nanoparticle including an organometallic sandwich compound and a magnetic metal oxide. The functionalized magnetic nanoparticle may be reacted with a metal precursor to form a catalyst for various C—C bond forming reactions. The catalyst may be recovered with ease by attracting the catalyst with a magnet.

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