Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

726796

Sigma-Aldrich

(S)-(+)-1-Cyclohexylethylamine

ChiPros®, produced by BASF, 99%

Synonym(s):

(S)-(+)-α-Methylcyclohexanemethylamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H11CH(CH3)NH2
CAS Number:
17430-98-7
Molecular Weight:
127.23
Beilstein:
2935069
MDL number:
MFCD00066261
UNSPSC Code:
12352116
PubChem Substance ID:
329764266
NACRES:
NA.22

grade

produced by BASF

Quality Level

100

Assay

≥98.5% (GC)
99%

form

liquid

optical purity

enantiomeric excess: ≥98.5%

refractive index

n20/D 1.4614 (lit.)

bp

60 °C/12 mmHg (lit.)

density

0.856 g/mL at 25 °C (lit.)

SMILES string

C[C@H](N)C1CCCCC1

InChI

1S/C8H17N/c1-7(9)8-5-3-2-4-6-8/h7-8H,2-6,9H2,1H3/t7-/m0/s1

InChI key

XBWOPGDJMAJJDG-ZETCQYMHSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(S)-(+)-1-Cyclohexylethylamine is a chiral amine.

Application

(S)-(+)-1-Cyclohexylethylamine may be used in the synthesis of (S)-(-)-ferrocenylimine by reacting with ferrocenecarboxaldehyde.

Legal Information

ChiPros is a registered trademark of BASF SE

Signal Word

Danger

Hazard Statements

H226,H314,H411

Hazard Classifications

Aquatic Chronic 2 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

125.6 °F - closed cup

Flash Point(C)

52 °C - closed cup

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCG5492
BCCC5336
BCCB5072
BCBV5981
BCBP2349V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Yee Voan Teo et al.
Cell reports, 27(4), 997-1007 (2019-04-25)
Oncogene-induced senescence (OIS) is a tumor suppressive response to oncogene activation that can be transmitted to neighboring cells through secreted factors of the senescence-associated secretory phenotype (SASP). Currently, primary and secondary senescent cells are not considered functionally distinct endpoints. Using
Chiral mono and diamide derivatives of calix [4] arene for enantiomeric recognition of chiral amines
Kocabas, Erdal, et al.
Chirality, 20.1, 26-34 (2008)
Isoindolinones via a room temperature palladium nanoparticle-catalysed 3-component cyclative carbonylation?amination cascade
Grigg, Ronald, et al.
Tetrahedron, 44.37, 6979-6982 (2003)
Expedient synthesis and design strategies for new peptoid construction
Gorske, Benjamin C., et al.
Organic Letters, 7.8, 1521-1524 (2005)
Synthesis of optically-active planar chiral derivatives of ferrocene. Crystal structures of alkyne insertion products.
Zhao G, et al.
Tetrahedron Asymmetry, 9(13), 2253-2257 (1998)
View All Related Papers

Articles

ChiPros Chiral Amines

ChiPros Chiral Amines

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