Chemical Properties of Prostaglandine F3A, cyclohexaneboronate

Prostaglandine F3A, cyclohexaneboronate

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InChI
InChI=1S/C26H41BO5/c1-2-3-7-14-21(28)17-18-23-22(15-10-4-5-11-16-26(29)30)24-19-25(23)32-27(31-24)20-12-8-6-9-13-20/h3-4,7,10,17-18,20-25,28H,2,5-6,8-9,11-16,19H2,1H3,(H,29,30)/b7-3-,10-4-,18-17+/t21-,22+,23+,24-,25+/m1/s1
InChI Key
JOUDZIRNFSJFAW-MJJIFDGMSA-N
Formula
C26H41BO5
SMILES
CCC=CCC(O)C=CC1C2CC(OB(C3CCCCC3)O2)C1CC=CCCCC(=O)O
Molecular Weight1
444.41
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Physical Properties

Property Value Unit Source
log10WS -5.01 Crippen Calculated Property
logPoct/wat 5.704 Crippen Calculated Property
Inp 3120.00 NIST

Similar Compounds

Prostaglandine F2A, cyclohexaneboronate. Prostaglandine F1A, cyclohexaneboronate. Prostaglandine F3A, butaneboronate. Prostaglandine F2A, butaneboronate. Prostaglandine F3A, methaneboronate. Prostaglandine F1A, butaneboronate. Prostaglandine F2A, methaneboronate. Prostaglandine F1A, methaneboronate. Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (19«alpha»)-. 1H-Indole-3-ethanol, 2-(5-ethenyl-1-azabicyclo[2.2.2]oct-2-yl)-, [1S-(1«alpha»,2«alpha»,4«alpha»,5«beta»)]-. Epibaptifoline. Baptifoline. Argentamin. Leu-Trp, N-trimethylsilyl-, trimethylsilyl ester. (1'S,3R,4a'S,5a'S,10a'S)-Methyl 1'-methyl-2-oxo-1',4a',5',5a',7',8',10',10a'-octahydrospiro[indoline-3,6'-pyrano[3,4-f]indolizine]-4'-carboxylate.

Find more compounds similar to Prostaglandine F3A, cyclohexaneboronate.

Sources

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