Chemical Properties of 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (OH-N-acetyl-), isomer 2, propionylated

4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (OH-N-acetyl-), isomer 2, propionylated

PDF Excel Molecule Calculator
InChI
InChI=1S/C17H25NO5/c1-6-13-14(21-4)10-12(8-9-18-11(3)19)16(22-5)17(13)23-15(20)7-2/h10H,6-9H2,1-5H3,(H,18,19)
InChI Key
UQHVBQZITCKPRN-UHFFFAOYSA-N
Formula
C17H25NO5
SMILES
CCC(=O)Oc1c(CC)c(OC)cc(CCNC(C)=O)c1OC
Molecular Weight1
323.38
Cheméo is a service of Céondo GmbH, since 2007, we provide simulation, modelling and software development services for the industry. Do not hesitate to contact us for your projects.

Physical Properties

Property Value Unit Source
Δf -317.30 kJ/mol Joback Calculated Property
Δfgas -771.91 kJ/mol Joback Calculated Property
Δfus 44.13 kJ/mol Joback Calculated Property
Δvap 85.52 kJ/mol Joback Calculated Property
log10WS -3.85 Crippen Calculated Property
logPoct/wat 2.260 Crippen Calculated Property
McVol 257.360 ml/mol McGowan Calculated Property
Pc 1611.58 kPa Joback Calculated Property
Inp [2570.00; 2570.00]   Show Hide
Inp 2570.00 NIST
Inp 2570.00 NIST
Tboil 860.13 K Joback Calculated Property
Tc 1066.30 K Joback Calculated Property
Tfus 577.06 K Joback Calculated Property
Vc 0.981 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [786.73; 852.64] J/mol×K [860.13; 1066.30] Show Hide
Cp,gas 786.73 J/mol×K 860.13 Joback Calculated Property
Cp,gas 800.66 J/mol×K 894.49 Joback Calculated Property
Cp,gas 813.42 J/mol×K 928.85 Joback Calculated Property
Cp,gas 825.01 J/mol×K 963.22 Joback Calculated Property
Cp,gas 835.43 J/mol×K 997.58 Joback Calculated Property
Cp,gas 844.64 J/mol×K 1031.94 Joback Calculated Property
Cp,gas 852.64 J/mol×K 1066.30 Joback Calculated Property

Similar Compounds

4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (HO-N-acetyl-), isomer 1, propionylated. 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (hydroxyl-N-acetyl)-isomer 2, acetylated. 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (hydroxyl-N-acetyl)-isomer 1, acetylated. 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (HO-N-acetyl-), 2TFA. 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (HO-), 2TFA. Phenethylamine, 2,5-dimethoxy-4-propylthio, N-acetyl, acetoxy-M. 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (O-desmethyl-N-acetyl)-isomer 2, acetylated. 2-(2-Acetoxy-5-methoxy-4-ethylphenyl)ethylamine, N-acetyl-. Phenethylamine, 2,5-dimethoxy-4-propylthio, N-acetyl, trifluoroacetoxy-M. 2,5-Dimethoxy-4-methyl-«beta»-phenethylamine-M (O-desmethyl-N-acetyl-), TFA, II. 4-iodo-2,5-dimethoxy-«beta»-phenethylamine-M, (O-desmethyl-), isomer 2, diacetylated. 4-iodo-2,5-dimethoxy-«beta»-phenethylamine-M, (O-desmethyl-), isomer 1, diacetylated. 2,5-Dimethoxy-4-methyl-«beta»-phenethylamine-M (O-desmethyl-N-acetyl-), TFA, I. 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (O-desmethyl), isomer 2, 2TFA. Phenethylamine, 2,5-dimethoxy-4-methylthio, sulfoxide, N-acetyl.

Find more compounds similar to 4-ethyl-2,5-dimethoxy-«beta»-phenethylamine-M, (OH-N-acetyl-), isomer 2, propionylated.

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.