Chemical Properties of Morpholine, N-isoBOC

Morpholine, N-isoBOC

InChI
InChI=1S/C9H17NO3/c1-8(2)7-13-9(11)10-3-5-12-6-4-10/h8H,3-7H2,1-2H3
InChI Key
XLDHZKAMJKEUNG-UHFFFAOYSA-N
Formula
C9H17NO3
SMILES
CC(C)COC(=O)N1CCOCC1
Molecular Weight1
187.24
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Physical Properties

Property Value Unit Source
ω 0.5673 Relay (1.0) Calculated Property
Δfgas -606.24 kJ/mol Relay (1.0) Calculated Property
Δvap 68.39 kJ/mol Relay (1.0) Calculated Property
IE 9.45 eV Relay (1.0) Calculated Property
log10WS -0.12 Relay (1.0) Calculated Property
logPoct/wat 1.111 Crippen Calculated Property
McVol 150.100 ml/mol McGowan Calculated Property
Pc 2463.91 kPa Relay (1.0-beta) Calculated Property
Inp 1370.00 NIST
Tboil 551.02 K Relay (1.0) Calculated Property
Tc 727.89 K Relay (1.0) Calculated Property
Tfus 245.88 K Relay (1.0) Calculated Property
Vc 0.561 m3/kmol Relay (1.0) Calculated Property

Cheméo can also estimate Standard Gibbs free energy of formation for this compound, but it falls outside the models' validated range, so it is not shown here. Open the prediction tool to compute it on demand.

Similar Compounds

Isobutylcarbamate, N,N-diethyl. Diethanolamine, N-isoBOC, O-TBDMS, # 1. bis O-TBDMS derivative of N-isoBOC diethanolamine. Glycine, N-methyl-N-propoxycarbonyl-, isobutyl ester. 4-Trichloroacetyl morpholine. Isobutylcarbamate, N-ethyl-N-methyl. Isobutylcarbamate, N,N-dipropyl. Sarcosylsarcosine, N-isobutoxycarbonyl-, ethyl ester. Glycine, N-methyl-N-ethoxycarbonyl-, isobutyl ester. Glycine, N-methyl-n-butoxycarbonyl-, isobutyl ester. Glycine, N-methyl-N-allyloxycarbonyl-, isobutyl ester. Isobutylcarbamate, N,Np-diisobutyl. Sarcosylsarcosine, N-isobutoxycarbonyl-, propyl ester. Pyrrolidine, N-isoBOC. Isobutylcarbamate, N,N-dibutyl.

Find more compounds similar to Morpholine, N-isoBOC.

Sources

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