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关于此项目
线性分子式:
C6H11CH(CH3)NH2
化学文摘社编号:
分子量:
127.23
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2935069
Assay:
≥98.5% (GC), 99%
Form:
liquid
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
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
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
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
125.6 °F - closed cup
flash_point_c
52 °C - closed cup
法规信息
危险化学品
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商品
Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 726796-25G | 04061832719986 |
| 726796-100G | 04061832719979 |


