E45708
1-Ethylpiperidine
99%
Synonym(s):
N-Ethylpiperidine, NSC 2090
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About This Item
Empirical Formula (Hill Notation):
C7H15N
CAS Number:
Molecular Weight:
113.20
Beilstein:
102643
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.444 (lit.)
bp
131 °C (lit.)
density
0.824 g/mL at 25 °C (lit.)
SMILES string
CCN1CCCCC1
InChI
1S/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H3
InChI key
HTLZVHNRZJPSMI-UHFFFAOYSA-N
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Application
Reactant for:
Synthesis of multiprotected kanosamine
Selective acylation in peptide synthesis
Reagent for:
Stereoselective aldol condensation reactions for synthesis of β-lactam antibiotics
Diastereoselective synthesis of aldols
Crossed Claisen ester condensation
Synthesis of multiprotected kanosamine
Selective acylation in peptide synthesis
Reagent for:
Stereoselective aldol condensation reactions for synthesis of β-lactam antibiotics
Diastereoselective synthesis of aldols
Crossed Claisen ester condensation
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
62.6 °F
Flash Point(C)
17 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Yoo Tanabe and Teruaki Mukaiyama
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Synthesis, 1, 161-167 (2011)
Mankil Jung and Marvin J. Miller
Tetrahedron Letters, 26, 977-980 (1985)
Amino-acids and peptides. XXIV. The use of esters of 1-hydroxypiperidine and of other NN-dialkylhydroxylamines in peptide synthesis and as selective acylating agents.
B O Handford et al.
Journal of the Chemical Society. Perkin transactions 1, Dec, 6814-6827 (1965-12-01)
Shigeki Sano et al.
Chemical & pharmaceutical bulletin, 50(9), 1300-1302 (2002-09-19)
Tetrasubstituted (Z)-alkenes were readily prepared through the Horner-Wadsworth-Emmons reactions of methyl 2-[bis(2,2,2-trifluoroethyl)phosphono]propionate with aryl alkyl ketones by employing Sn(OSO(2)CF(3))(2) and N-ethylpiperidine.
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