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About This Item
Empirical Formula (Hill Notation):
C9H12N2
CAS Number:
Molecular Weight:
148.20
Beilstein:
472443
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
purum
Quality Level
Assay
≥98.0% (NT)
form
crystals
mp
54-58 °C (lit.)
55-61 °C
solubility
methanol: 0.1 g/mL, clear
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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Related Categories
Other Notes
Hypernucleophilic acylation catalyst. Reviews
Signal Word
Danger
Hazard Statements
Precautionary Statements
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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A. Hassner
Tetrahedron, 34, 2069-2069 (1978)
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.
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)
E.F. Scriven
Chemical Society Reviews, 12, 129-129 (1983)
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