83300
2-Pyrrolidinone
purum, ≥98.0% (GC)
Sinónimos:
2-Pyrrolidone, Butyrolactam
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Fórmula empírica (notación de Hill):
C4H7NO
Número CAS:
Peso molecular:
85.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-483-1
Beilstein/REAXYS Number:
105241
MDL number:
Assay:
≥98.0% (GC)
Form:
solid
Servicio técnico
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Permítanos ayudarlevapor density
2.9 (vs air)
Quality Level
grade
purum
assay
≥98.0% (GC)
form
solid
refractive index
n20/D 1.487 (lit.)
bp
245 °C (lit.)
mp
23-25 °C (lit.)
solubility
H2O: miscible (completely)
density
1.12 g/mL at 25 °C (lit.)
SMILES string
O=C1CCCN1
InChI
1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)
InChI key
HNJBEVLQSNELDL-UHFFFAOYSA-N
Gene Information
rat ... Gabra2(29706)
Application
- 2-Pyrrolidinone is used in the synthesis of N-vinylpyrrolidone, from which polyvinylpyrrolidone (PVP) is obtained.
- It can be used as a ligand in the preparation of one-dimensional coordination polymers and mixed transition metal-lanthanide complexes.
- 1,2-amino alcohols can be reacted with carbon dioxide in the presence of 2-pyrrolidinone electrogenerated base to synthesize various oxazolidin-2-ones (Evans-type auxiliaries).
- It is a key starting material in the synthesis of (±)-tetraponerine T4.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Repr. 1B
Clase de almacenamiento
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Syntheses, structures and magnetic properties of 1-D coordination polymers containing both dicyanamide and 2-pyrrolidone.
Sun B W, et al.
Inorganic Chemistry Communications, 4(2), 72-75 (2001)
Mixed Transition Metal? Lanthanide Complexes at High Oxidation States: Heteronuclear CeIVMnIV Clusters.
Tasiopoulos A J, et al.
Inorganic Chemistry, 46(23), 9678-9691 (2007)
The reaction of 1, 2-amino alcohols with carbon dioxide in the presence of 2-pyrrolidone electrogenerated base. New synthesis of chiral oxazolidin-2-ones.
Casadei M A, et al.
The Journal of Organic Chemistry, 65(15), 4759-4761 (2000)