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Merck
CN

726796

(S)-(+)-1-Cyclohexylethylamine

ChiPros®, produced by BASF, 99%

Synonym(s):

(S)-(+)-α-Methylcyclohexanemethylamine

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About This Item

Linear Formula:
C6H11CH(CH3)NH2
CAS Number:
17430-98-7
Molecular Weight:
127.23
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
329764266
MDL number:
MFCD00066261
Beilstein/REAXYS Number:
2935069
Assay:
≥98.5% (GC), 99%
Form:
liquid

Key Documents

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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

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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

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
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Certificates of Analysis (COA)

Lot/Batch Number
BCCG5492
BCCC5336
BCCB5072
BCBV5981
BCBP2349V

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Supramolecular chirogenesis in bis (zinc porphyrin): an absolute configuration probe highly sensitive to guest structure
Borovkov, Victor V., Juha M. Lintuluoto, and Yoshihisa Inoue
Organic Letters, 2.11, 1565-1568 (2000)
Expedient synthesis and design strategies for new peptoid construction
Gorske, Benjamin C., et al.
Organic Letters, 7.8, 1521-1524 (2005)
Isoindolinones via a room temperature palladium nanoparticle-catalysed 3-component cyclative carbonylation?amination cascade
Grigg, Ronald, et al.
Tetrahedron, 44.37, 6979-6982 (2003)
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)
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Articles

ChiPros Chiral Amines

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

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