56210
3-Hydroxypiperidine
≥98.0% (NT)
Synonym(s):
3-Piperidinol
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About This Item
Empirical Formula (Hill Notation):
C5H11NO
CAS Number:
Molecular Weight:
101.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
229-957-4
Beilstein/REAXYS Number:
102696
MDL number:
Assay:
≥98.0% (NT)
Form:
solid
InChI
1S/C5H11NO/c7-5-2-1-3-6-4-5/h5-7H,1-4H2
InChI key
BIWOSRSKDCZIFM-UHFFFAOYSA-N
SMILES string
OC1CCCNC1
assay
≥98.0% (NT)
form
solid
mp
57-61 °C
solubility
H2O: 1 g/mL, clear
functional group
hydroxyl
storage temp.
2-8°C
Quality Level
Related Categories
General description
3-Hydroxypiperidine can be obtained from the reduction of 3-hydroxypyridine.
Application
3-Hydroxypiperidine may be used to synthesize the following:
- 2-pyrrolidinone via oxidation with iodosylbenzene
- 1-[2,8-bis(trifluoromethyl)quinolin-4-yl]piperidin-3-ol via reaction with 4-bromoquinoline
Reactant for:
Synthesis of unsymmetrical ureas
Synthesis of piperidine nucleoside analogs
Fluorination reactions
Synthesis of substituted pyridines
Synthesis of unsymmetrical ureas
Synthesis of piperidine nucleoside analogs
Fluorination reactions
Synthesis of substituted pyridines
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Synthesis of quinoline analogs: search for antimalarial agents
Babu R K, et al.
Monatshefte fur Chemie / Chemical Monthly, 139(2), 179-181 (2008)
Oxidation of 3-hydroxypiperidines with iodosylbenzene in water: Tandem oxidative Grob fragmentation-cyclization reaction
Tada N, et al.
Chemical & Pharmaceutical Bulletin, 52(9), 1143-1144 (2004)
Katritzky.RA, et al.
Comprehensive Organic Functional Group Transformations II, 1 (1995)
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