Chemical Properties of Galvinoxyl radical

Galvinoxyl radical

InChI
InChI=1S/C29H41O2/c1-18(2)9-24-14-22(15-25(28(24)30)10-19(3)4)13-23-16-26(11-20(5)6)29(31)27(17-23)12-21(7)8/h13-21H,9-12H2,1-8H3
InChI Key
GOVAISVZGLQKDS-UHFFFAOYSA-N
Formula
C29H41O2
SMILES
CC(C)CC1=CC(=Cc2cc(CC(C)C)c([O])c(CC(C)C)c2)C=C(CC(C)C)C1=O
Molecular Weight1
421.64
Other Names
  • Galvinoxyl radical
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Physical Properties

Property Value Unit Source
logPoct/wat 8.139 Crippen Calculated Property
McVol 377.240 ml/mol McGowan Calculated Property
solid,1 bar 670.10 J/mol×K NIST

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Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,solid 654.28 J/mol×K 298.15 NIST

Similar Compounds

Quinidine. Quinine. Estra-1,3,5(10)-trien-17-one, 1-methyl-3,6,7-tris[(trifluoroacetyl)oxy]-, (6«alpha»,7«alpha»)-. ethyl eburnamenine-14-carboxylate. norbormide. Rotenone. Spiro[2H-1-benzopyran-2,2'-[2H]indole], 1',3'-dihydro-1',3',3'-trimethyl-6-nitro-. (1,S,2S,3R,5S)-(+)-Pinanediol, , 2-(N,N-dimethylaminomethyl)-ferroceneboronate. Etorphine. Morphinan-3,6-diol, 7,8-didehydro-4,5-epoxy-17-methyl- (5«alpha»,6«alpha»)-, bis(trifluoroacetate) (ester). [2,2'-Bimorphinan]-3,3',6,6'-tetrol, 7,7',8,8'-tetradehydro-4,5:4',5'-diepoxy-17,17'-dimethyl-, (5«alpha»,6«alpha»)-(5'«alpha»,6'«alpha»)-. Dihydrocodeine tms derivative. Xanthine riboside, TMS. Hydromorphone, trimethylsilyl ether. Hydromorphone, tert-butyldimethylsilyl ether.

Find more compounds similar to Galvinoxyl radical.

Sources

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