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Molecule
ID:112050
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₇H₂₃NO₃
Molecular Mass
289.36942
Exact Mass
289.1677936
Charge
0
InChI
InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15?,16-/m1/s1
InChIKey
RKUNBYITZUJHSG-VFSICIBPSA-N
Canonic Smiles
OC[C@H](c1ccccc1)C(=O)OC1C[C@@H]2CC[C@H](C1)N2C
Isomeric Smiles
CN1[C@H]2CC[C@@H]1CC(C2)OC(=O)[C@H](CO)c1ccccc1
Calculated Properties
JChem
Acid pKa
15.1457405
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.7801015
LogD (pH = 7.4)
-0.40574417
Log P
1.571241
Molar Refractivity
80.8164
Polarizability
32.034832
Polar Surface Area
49.77
Rotatable Bonds
5
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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MP Biomedicals
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Data Source
Commercial Catalog
MP Biomedicals
05222337
Academic Data
PubChem
154417
Names and Identifiers
Synonyms
L-HYOSCYAMINE
IUPAC Traditional name
(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-3-hydroxy-2-phenylpropanoate
IUPAC name
(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-3-hydroxy-2-phenylpropanoate
Registration numbers
CAS Number
101-31-5
PubChem CID
154417
PubChem SID
162096827
Properties
Safety Information
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Product Information
Certificate of Analysis
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Molecule Details
MP Biomedicals
05222337
MP Biomedicals Rare Chemical collection
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay