Names | |
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IUPAC name
4-pyrrolidin-1-ylpyridine
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Other names
4-(1-pyrrolidinyl)pyridine
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Identifiers | |
3D model (
JSmol)
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ChemSpider | |
ECHA InfoCard | 100.017.759 |
EC Number |
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PubChem
CID
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|
UNII | |
CompTox Dashboard (
EPA)
|
|
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| |
Properties | |
C9H12N2 | |
Molar mass | 148.209 g·mol−1 |
Appearance | white solid |
Melting point | 55–56 °C (131–133 °F; 328–329 K) |
Boiling point | 170–171 °C (338–340 °F; 443–444 K) 12 TTor |
Hazards | |
GHS labelling: | |
Danger | |
H301, H314 | |
P260, P264, P270, P280, P301+P310, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
4-Pyrrolidinylpyridine is an organic compound with the formula (CH2)4NC5H4N. The molecule consists of a pyrrodinyl group ((CH2)4N-) attached via N to the 4-position of pyridine. It is a white solid. The compound has attracted interest because it (pKa = 9.58) is more basic than dimethylaminopyridine (pKa = 9.41). [1] It is a popular base catalyst. [2]
Names | |
---|---|
IUPAC name
4-pyrrolidin-1-ylpyridine
| |
Other names
4-(1-pyrrolidinyl)pyridine
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.017.759 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C9H12N2 | |
Molar mass | 148.209 g·mol−1 |
Appearance | white solid |
Melting point | 55–56 °C (131–133 °F; 328–329 K) |
Boiling point | 170–171 °C (338–340 °F; 443–444 K) 12 TTor |
Hazards | |
GHS labelling: | |
Danger | |
H301, H314 | |
P260, P264, P270, P280, P301+P310, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
4-Pyrrolidinylpyridine is an organic compound with the formula (CH2)4NC5H4N. The molecule consists of a pyrrodinyl group ((CH2)4N-) attached via N to the 4-position of pyridine. It is a white solid. The compound has attracted interest because it (pKa = 9.58) is more basic than dimethylaminopyridine (pKa = 9.41). [1] It is a popular base catalyst. [2]