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Merck
CN

179604

Sigma-Aldrich

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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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.)

SMILES string

N[C@@H]1C[C@H]2CC[C@@H]1C2

InChI

1S/C7H13N/c8-7-4-5-1-2-6(7)3-5/h5-7H,1-4,8H2/t5-,6+,7+/m0/s1

InChI key

JEPPYVOSGKWVSJ-RRKCRQDMSA-N

General description

exo-2-Aminonorbornane is an inhibitor of putrescine N-methyltransferase. The structural and conformational properties of exo-2-aminonorbornane was studied.

Pictograms

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Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

95.0 °F - closed cup

Flash Point(C)

35 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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