186112
N-(3-Aminopropyl)-2-pipecoline
96%
Synonym(s):
1-(3-Aminopropyl)-2-methylhexahydropyridine, 2-Methyl-1-piperidinepropanamine
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About This Item
Empirical Formula (Hill Notation):
C9H20N2
CAS Number:
Molecular Weight:
156.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
96%
form
liquid
refractive index
n20/D 1.4765 (lit.)
bp
96-97 °C/15 mmHg (lit.)
density
0.889 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CC1CCCCN1CCCN
InChI
1S/C9H20N2/c1-9-5-2-3-7-11(9)8-4-6-10/h9H,2-8,10H2,1H3
InChI key
YYAYTNPNFKPFNG-UHFFFAOYSA-N
Application
N-(3-Aminopropyl)-2-pipecoline was used as internal standard during the determination of arginine, agmatine and their metabolites by HPLC. It was used in the synthesis of novel piperidinylethyl, phenoxyethyl and fluoroethyl thiourea compounds having anti-HIV activity.
Reactant for synthesis of:
Photostable near-infrared cyanine dyes
Quinazolindione derivatives as 5-HT3A receptor antagonists
Melanocortin-4 receptor antagonists
Brain penetrant aminoalkyl benzoimidazoles
Selective nitric oxide formation inhibitors
Photostable near-infrared cyanine dyes
Quinazolindione derivatives as 5-HT3A receptor antagonists
Melanocortin-4 receptor antagonists
Brain penetrant aminoalkyl benzoimidazoles
Selective nitric oxide formation inhibitors
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
190.4 °F - closed cup
Flash Point(C)
88 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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John E Piletz et al.
Neurotoxicity research, 24(2), 176-190 (2013-01-22)
Agmatine is an endogenous brain metabolite, decarboxylated arginine, which has neuroprotective properties when injected intraperitoneally (i.p.) into rat pups following hypoxic-ischemia. A previous screen for compounds based on rat brain lysates containing agmatinase with assistance from computational chemistry, led to
T K Venkatachalam et al.
Antiviral chemistry & chemotherapy, 11(5), 329-336 (2001-01-06)
Derivatives of piperidinylethyl, phenoxyethyl and fluoroethyl bromopyridyl thioureas were designed and synthesized as non-nucleoside reverse transcriptase inhibitors (NNRTIs) of HIV-1 reverse transcriptase (RT). The anti-HIV activity of these compounds was examined by determining their ability to inhibit the replication of
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