179604
exo-2-Aminonorbornane
99%
Synonym(s):
exo-2-Norbornanamine
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About This Item
Empirical Formula (Hill Notation):
C7H13N
CAS Number:
Molecular Weight:
111.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-647-6
MDL number:
InChI key
JEPPYVOSGKWVSJ-RRKCRQDMSA-N
InChI
1S/C7H13N/c8-7-4-5-1-2-6(7)3-5/h5-7H,1-4,8H2/t5-,6+,7+/m0/s1
SMILES string
N[C@@H]1C[C@H]2CC[C@@H]1C2
assay
99%
form
liquid
refractive index
n20/D 1.4807 (lit.)
bp
49 °C/10 mmHg (lit.)
density
0.938 g/mL at 25 °C (lit.)
General description
exo-2-Aminonorbornane is an inhibitor of putrescine N-methyltransferase. The structural and conformational properties of exo-2-aminonorbornane was studied.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
95.0 °F - closed cup
flash_point_c
35 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Patricia Écija et al.
The Journal of chemical physics, 134(16), 164311-164311 (2011-05-03)
The intrinsic conformational and structural properties of the bicycle exo-2-aminonorbornane have been probed in a supersonic jet expansion using Fourier-transform microwave (FT-MW) spectroscopy and quantum chemical calculations. The rotational spectrum revealed two different conformers arising from the internal rotation of
N Hibi et al.
Plant physiology, 100(2), 826-835 (1992-10-01)
Biosynthesis of tropane alkaloids is thought to proceed by way of the diamine putrescine, followed by its methylation by putrescine N-methyltransferase (PMT; EC 2.1.1.53). High PMT activities were found in branch roots and/or cultured roots of several solanaceous plants. PMT
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