Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

344125

Sigma-Aldrich

(R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine

97%

Sign Into View Organizational & Contract Pricing

Synonym(s):
(R)-Ugi′s amine, (R)-(+)-[1-(Dimethylamino)ethyl]ferrocene
Empirical Formula (Hill Notation):
C14H19FeN
CAS Number:
Molecular Weight:
257.15
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

liquid

optical activity

[α]20/D +13°, c = 1 in ethanol (5 h)

refractive index

n20/D 1.589 (lit.)

bp

120-121 °C/0.7 mmHg (lit.)

density

1.222 g/mL at 20 °C (lit.)

SMILES string

[Fe].[CH]1[CH][CH][CH][CH]1.C[C@H]([C]2[CH][CH][CH][CH]2)N(C)C

InChI

1S/C9H14N.C5H5.Fe/c1-8(10(2)3)9-6-4-5-7-9;1-2-4-5-3-1;/h4-8H,1-3H3;1-5H;/t8-;;/m1../s1

InChI key

ISOLNZQTVMCEOI-YCBDHFTFSA-N

Looking for similar products? Visit Product Comparison Guide

Application

(R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine may be used as a starting material to synthesize:
  • chiral 1,2-disubstituted ferrocenyl amino alcohols
  • ferrocene-based P-chiral phosphine ligands
  • optically active α-ferrocenyl tertiary amines
Ligand used in the preparation of chiral allylic alcohols, axially chiral allenecarboxylic esters, and rhodium(I)-catalyzed asymmetric hydrosilylation of ketones.

WGK

WGK 3

Flash Point(F)

235.4 °F

Flash Point(C)

113 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Nishibayashi, Y. et al.
Tetrahedron Letters, 35, 3115-3115 (1994)
Nishibayashi, Y.et al.
Journal of the Chemical Society. Chemical Communications, 1375-1375 (1994)
Chiba, T. et al.
Tetrahedron Letters, 36, 1519-1519 (1995)
Stereoselective synthesis. VIII. Absolute configuration of a 1, 2-disubstituted ferrocene derivative with planar and central elements of chirality and the mechanism of the optically active. alpha.-ferrocenyl tertiary amines.
Battelle LF, et al.
Journal of the American Chemical Society, 95(2), 482-486 (1973)
Chiral auxiliaries for asymmetric synthesis: enantioselective addition of dialkylzincs to aldehydes catalyzed by chiral 1, 2-disubstituted ferrocenyl amino alcohols.
Watanabe M, et al.
The Journal of Organic Chemistry, 56(6), 2218-2224 (1991)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service