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Molecule
ID:53612
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₅NO
Molecular Mass
141.2108
Exact Mass
141.11536411
Charge
0
InChI
InChI=1S/C8H15NO/c1-9-6-2-3-7(9)5-8(10)4-6/h6-8,10H,2-5H2,1H3
InChIKey
CYHOMWAPJJPNMW-UHFFFAOYSA-N
Canonic Smiles
OC1CC2CCC(C1)N2C
Isomeric Smiles
N1(C2CC(CC1CC2)O)C
Calculated Properties
JChem
Acid pKa
15.160811
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-3.3879304
LogD (pH = 7.4)
-2.2382734
Log P
0.033560663
Molar Refractivity
40.5938
Polarizability
16.15159
Polar Surface Area
23.47
Rotatable Bonds
0
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02104921
InterBioScreen
BB_NC-0109
Matrix Scientific
058452
TRC
T892665
Bide Pharmatech
BD10735
Alfa Aesar
L02332
A&J Pharmtech
AJA-O5126
Academic Data
Wikipedia
Tropine
PubChem
8424
Names and Identifiers
IUPAC Traditional name
tropine
tropin
Synonyms
α-Tropine
TROPINE
Tropanol
8-Methyl-8-azabicyclo[3.2.1]octan-3-ol
endo-8-Methyl-8-azabicyclo[3.2.1]-octan-3-ol
3-Tropanol
Tropine
品托碱
endo-8-Methyl-8-azabicyclo[3.2.1]octan-3-ol
N-Methyl-8-azabicyclo[3.2.1]octan-3-ol
endo-Tropanol
2,3-Dihydro-3α-hydroxy-8-methylnortropidine
3-exo-8-Methyl-8-azabicyclo[3.2.1]octan-3-ol
2,3-Dihydro-3α-hydroxytropidine
(1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-ol
(3-endo)-8-Methyl-8-azabicyclo[3.2.1]octan-3-ol
IUPAC name
8-methyl-8-azabicyclo[3.2.1]octan-3-ol
Registration numbers
CAS Number
120-29-6
135-97-7
PubChem CID
8424
Wikipedia Title
Tropine
Unique Ingredient Identifier
7YXR19M72Y
MeSH Name
Tropine
Merck Index
149781
MDL Number
MFCD00005551
MFCD00180667
EC Number
204-384-2
Beilstein Number
80188
PubChem SID
162058375
Molecule Details
Wikipedia
Tropine
TRC
T892665
An oxidative product of Tropane, used to synthesize alkaloid derivatives.
References
PubChem Literature
From Data Sources
•
Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010)
•
Kok, G., et al.: Bioorg. Med. Chem. Lett., 20, 4499 (2010)
•
Schmitt, K., et al.: J. Neurochem., 115, 296 (2010)
Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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PubChem CID
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Wikipedia Title
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Unique Ingredient Identifier
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MeSH Name
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Merck Index
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PubChem SID
Properties
Safety Information
MSDS Link
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Source
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Source
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TSCA Listed
false
Source
是
Source
IRRITANT
Source
Hygroscopic
Source
2-8°C
Source
Refrigerator
Source
YM3875000
Source
Harmful (X)
P261
-
P301+P310
-
P321
-
P304+P340
-
P405
-P501A
Source
36
Source
H301
-
H332
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
20/22
Source
Product Information
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98%
Source
97%
Source
Physical Property
233°C
Source
232-234°C
Source
Hygroscopic plates
Source
White SolidOff-White Solid
Source
1.016 g/cm
3
at 100 °C
Source
1.04
Source
Source
Source
Very soluble in water, diethyl ether, ethanol
Source
Methanol
Source
Chloroform
Source
Water
Source
64°C
Source
50-52°C
Source
61-65°C (dried)
Source
Storage Warning
Storage Condition
RTECS
European Hazard Symbols
GHS Precautionary statements
Safety Statements
GHS Hazard statements
GHS Pictograms
Risk Statements
Certificate of Analysis
Purity
Boiling Point
Apperance
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Melting Point