Chemical Properties of 2-Aminophenol, N,O-di(tert.-butyldimethylsilyl)-

2-Aminophenol, N,O-di(tert.-butyldimethylsilyl)-

InChI
InChI=1S/C18H35NOSi2/c1-17(2,3)21(7,8)19-15-13-11-12-14-16(15)20-22(9,10)18(4,5)6/h11-14,19H,1-10H3
InChI Key
YEPZRRKUCHNPJQ-UHFFFAOYSA-N
Formula
C18H35NOSi2
SMILES
CC(C)(C)[Si](C)(C)Nc1ccccc1O[Si](C)(C)C(C)(C)C
Molecular Weight1
337.65
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Physical Properties

Property Value Unit Source
ω 0.5996 Relay (1.0) Calculated Property
Δf 160.16 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas -469.26 kJ/mol Relay (1.0) Calculated Property
Δvap 68.60 kJ/mol Relay (1.0) Calculated Property
IE 7.51 eV Relay (1.0) Calculated Property
log10WS -4.56 Relay (1.0) Calculated Property
logPoct/wat 6.488 Crippen Calculated Property
Pc 1656.93 kPa Relay (1.0-beta) Calculated Property
Inp [1915.00; 1923.00]   Show Hide
Inp 1923.00 NIST
Inp 1915.00 NIST
Tboil 564.07 K Relay (1.0) Calculated Property
Tc 824.64 K Relay (1.0) Calculated Property
Tfus 342.84 K Relay (1.0) Calculated Property
Vc 1.122 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

2-Amino-4-nitrophenol, N,O-bis(tert-butyldimethylsilyl)-. 2-(N-tert-Butyldimethylsilyl)amino-4-methylphenol tert-butyldimethylsilyl ether. 4-Aminophenol, N,O-bis(tert-butyldimethylsilyl)-. 5-Amino-2-methoxyphenol, N-tert-butyldimethylsilyl-, tert-butyldimethylsilyl ether. 3-(tert-Butyldimethylsilyloxy)-4-methyl-N-(tert-butyldimethylsilyl)aniline. xanthosine-5'-monophosphate, TMS. Quinine, trimethylsilyl ether. Hypoxanthine-7-ethanol, 2,3-dihydro-3-(diphenylmethyl)-, acetate. 9H-Purin-2-amine, N-(trimethylsilyl)-6-[(trimethylsilyl)oxy]-9-[2,3,5-tris-O-(trimethylsilyl)-«beta»-D-ribofuranosyl]-. Cytidine, metho-oxime-TMS derivative. 9H-purine-6(1h)-thione, 9-beta-d-ribofuranosyl-, 2',3'-diacetate, 5'-bis(3,5-dimethylphenyl)phosphate. Moexipril Me. (E)-Eruciflorine. Acetylgynuramine. 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 2-Aminophenol, N,O-di(tert.-butyldimethylsilyl)-.

Sources

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