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
ω 1.0219 Relay (... Calculated Property
ΔfG° -224.97 kJ/mol Relay (... Calculated Property ⚠️
ΔfH°gas -1154.11 kJ/mol Relay (... Calculated Property
ΔvapH° 165.01 kJ/mol Relay (... Calculated Property
IE 8.67 eV Relay (... Calculated Property
log10WS -4.39 Relay (... Calculated Property
logPoct/wat 5.704 Crippen Calculated Property
Pc 349.66 kPa Relay (... Calculated Property ⚠️
Inp 3120.00 NIST
Tboil 736.59 K Relay (... Calculated Property
Tc 1005.26 K Relay (... Calculated Property
Tfus 447.76 K Relay (... Calculated Property
Vc 1.275 m3/kmol Relay (... Calculated Property

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. Epibaptifoline. 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. Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (19«alpha»)-. Baptifoline. 1H-Indole-3-ethanol, 2-(5-ethenyl-1-azabicyclo[2.2.2]oct-2-yl)-, [1S-(1«alpha»,2«alpha»,4«alpha»,5«beta»)]-.

Find more compounds similar to Prostaglandine F3A, cyclohexaneboronate.

Sources

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