Skip to Content
Merck
CN

726796

(S)-(+)-1-Cyclohexylethylamine

ChiPros®, produced by BASF, 99%

Synonym(s):

(S)-(+)-α-Methylcyclohexanemethylamine

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
C6H11CH(CH3)NH2
CAS Number:
Molecular Weight:
127.23
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2935069
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

(S)-(+)-1-Cyclohexylethylamine, ChiPros®, produced by BASF, 99%

InChI

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

SMILES string

C[C@H](N)C1CCCCC1

InChI key

XBWOPGDJMAJJDG-ZETCQYMHSA-N

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.)

functional group

amine

Looking for similar products? Visit Product Comparison Guide

Application

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

General description

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

Legal Information

ChiPros is a registered trademark of BASF SE

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

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
Isoindolinones via a room temperature palladium nanoparticle-catalysed 3-component cyclative carbonylation?amination cascade
Grigg, Ronald, et al.
Tetrahedron, 44.37, 6979-6982 (2003)
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)
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)
Expedient synthesis and design strategies for new peptoid construction
Gorske, Benjamin C., et al.
Organic Letters, 7.8, 1521-1524 (2005)

Articles

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

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