83275
4-吡咯烷基吡啶
purum, ≥98.0% (NT)
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经验公式（希尔记法）:
C9H12N2
化学文摘社编号:
分子量:
148.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-534-2
Beilstein/REAXYS Number:
472443
MDL number:
产品名称
4-吡咯烷基吡啶, purum, ≥98.0% (NT)
InChI key
RGUKYNXWOWSRET-UHFFFAOYSA-N
InChI
1S/C9H12N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h3-6H,1-2,7-8H2
SMILES string
C1CCN(C1)c2ccncc2
grade
purum
assay
≥98.0% (NT)
form
crystals
mp
54-58 °C (lit.)
55-61 °C
solubility
methanol: 0.1 g/mL, clear
Quality Level
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Other Notes
超强亲核酰化反应催化剂。综述
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Skin Corr. 1B
存储类别
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
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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
A. Hassner
Tetrahedron, 34, 2069-2069 (1978)
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.
E.F. Scriven
Chemical Society Reviews, 12, 129-129 (1983)
A method for the synthesis of isomerically pure saturated mixed-chain phosphatidylcholines.
J T Mason et al.
Analytical biochemistry, 113(1), 96-101 (1981-05-01)
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