Chemical Properties of 5-Hydroxyindoleacetic acid, ethoxycarbonylated, TBDMS

5-Hydroxyindoleacetic acid, ethoxycarbonylated, TBDMS

InChI
InChI=1S/C25H41NO5Si2/c1-12-29-23(28)26-17-18(15-22(27)31-33(10,11)25(5,6)7)20-16-19(13-14-21(20)26)30-32(8,9)24(2,3)4/h13-14,16-17H,12,15H2,1-11H3
InChI Key
UKRRCJNYBUNIEU-UHFFFAOYSA-N
Formula
C25H41NO5Si2
SMILES
CCOC(=O)n1cc(CC(=O)O[Si](C)(C)C(C)(C)C)c2cc(O[Si](C)(C)C(C)(C)C)ccc21
Molecular Weight1
491.77
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Physical Properties

Property Value Unit Source
ω 0.9944 Relay (1.0) Calculated Property
ΔfG° -236.17 kJ/mol Relay (1.0-beta) Calculated Property
ΔfH°gas -1182.44 kJ/mol Relay (1.0) Calculated Property
ΔvapH° 102.02 kJ/mol Relay (1.0) Calculated Property
IE 7.78 eV Relay (1.0) Calculated Property
log10WS -5.63 Relay (1.0) Calculated Property
logPoct/wat 7.121 Crippen Calculated Property
Pc 642.98 kPa Relay (1.0-beta) Calculated Property
Inp 2685.00 NIST
Tboil 704.62 K Relay (1.0) Calculated Property
Tc 966.25 K Relay (1.0) Calculated Property
Tfus 384.76 K Relay (1.0) Calculated Property
Vc 1.521 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

1H-Indole-3-ethanol, 2-(5-ethenyl-1-azabicyclo[2.2.2]oct-2-yl)-, [1S-(1«alpha»,2«alpha»,4«alpha»,5«beta»)]-. inosine-5'-monophosphate, TMS. xanthosine-5'-monophosphate, TMS. Quinine, trimethylsilyl ether. Poligodial + o-Tyr (ethyl ester) adduct (R,S), acetylated, # 1. 9H-purine-6(1h)-thione, 9-beta-d-ribofuranosyl-, 2',3'-diacetate, 5'-bis(3,5-dimethylphenyl)phosphate. Poligodial + o-Tyr (ethyl ester) adduct (R,S), acetylated, # 2. N6-TFA-2'-Deoxyadenosine, 3'-O-TFA, 5'-O-TBDMS. (E)-Cnidimine. N6-TFA-2'-Deoxyadenosine, 3'-O-TBDMS, 5'-O-TFA. (Z)-Cnidimine. xanthosine, TMS. 3-Indolepropionic acid, ethoxycarbonylated, TBDMS. Hydromorphone, trimethylsilyl ether. Etorphine.

Find more compounds similar to 5-Hydroxyindoleacetic acid, ethoxycarbonylated, TBDMS.

Sources

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