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213373

Sigma-Aldrich

4-Pyrrolidinopyridine

98%

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About This Item

Empirical Formula (Hill Notation):
C9H12N2
CAS Number:
2456-81-7
Molecular Weight:
148.20
Beilstein:
472443
EC Number:
219-534-2
MDL number:
MFCD00006415
UNSPSC Code:
12352005
PubChem Substance ID:
24852778
NACRES:
NA.22

Quality Level

200

Assay

98%

form

solid

mp

54-58 °C (lit.)

SMILES string

C1CCN(C1)c2ccncc2

InChI

1S/C9H12N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h3-6H,1-2,7-8H2

InChI key

RGUKYNXWOWSRET-UHFFFAOYSA-N

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Application

Catalyst employed in polymerization reactions. Ligand in metal complexes.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H314

Hazard Classifications

Acute Tox. 3 Oral - Skin Corr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ5657
BCCG9248
BCCF4186
BCCB4143
BCBM9852V

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Polymer, 34, 1297-1297 (1993)
Journal of Applied Polymer Science. Applied Polymer Symposium, 50, 149-149 (1993)
Polyhedron, 12, 689-689 (1993)
Brian L Hodous et al.
Journal of the American Chemical Society, 124(34), 10006-10007 (2002-08-22)
The first method for the catalytic enantioselective addition of amines (specifically, pyrroles) to ketenes has been developed, and it has been demonstrated that the resulting acylpyrroles can be transformed into a broad spectrum of useful derivatives. On the basis of
H Kai et al.
The Journal of pharmacy and pharmacology, 48(1), 53-56 (1996-01-01)
We have examined the effects of pyridine derivatives on phosphatidylcholine secretion in primary cultures of rat type II pneumocytes. Of 12 pyridine derivatives, 4-aminopyridine, 4-dimethylaminopyridine and 4-pyrolidinopyridine had a stimulatory effect on phosphatidylcholine secretion, whereas other derivatives had little effect.
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