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Molecule
ID:105493
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₅H₃₆O₃
Molecular Mass
384.55154
Exact Mass
384.26644501
Charge
0
InChI
InChI=1S/C25H36O3/c1-3-4-5-6-7-24(27)28-23-13-12-22-21-10-8-17-16-18(26)9-11-19(17)20(21)14-15-25(22,23)2/h9,11,16,20-23,26H,3-8,10,12-15H2,1-2H3
InChIKey
RFWTZQAOOLFXAY-UHFFFAOYSA-N
Canonic Smiles
CCCCCCC(=O)OC1CCC2C1(C)CCC1C2CCc2c1ccc(c2)O
Isomeric Smiles
CCCCCCC(=O)OC1CCC2C3CCc4c(ccc(O)c4)C3CCC12C
Calculated Properties
JChem
Acid pKa
10.327061
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
6.665431
LogD (pH = 7.4)
6.6649265
Log P
6.665437
Molar Refractivity
112.0871
Polarizability
44.347862
Polar Surface Area
46.53
Rotatable Bonds
7
Lipinski's Rule of Five
false
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Molecule Details
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Data Source
Academic Data
PubChem
3590886
Commercial Catalog
MP Biomedicals
02190414
Names and Identifiers
IUPAC Traditional name
5-hydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),3,5-trien-14-yl heptanoate
Synonyms
β-ESTRADIOL-17-ENANTHATE
IUPAC name
5-hydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),3,5-trien-14-yl heptanoate
Registration numbers
CAS Number
4956-37-0
EC Number
225-599-8
PubChem SID
162092133
PubChem CID
3590886
Properties
Product Information
Certificate of Analysis
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Purity
~98%
Source
Safety Information
Storage Condition
Room Temperature (15-30°C)
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MSDS Link
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References
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Bioactivity
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