Chemical Properties of 2(1H)-Naphthalenone, 6-methoxy

2(1H)-Naphthalenone, 6-methoxy

InChI
InChI=1S/C11H10O2/c1-13-11-5-3-8-6-10(12)4-2-9(8)7-11/h2-5,7H,6H2,1H3
InChI Key
YZHYNPBFYMUMNU-UHFFFAOYSA-N
Formula
C11H10O2
SMILES
COc1ccc2c(c1)C=CC(=O)C2
Molecular Weight1
174.20
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
ω 0.5078 Relay (1.0) Calculated Property
Δf -6.38 kJ/mol Joback Calculated Property
Δfgas -131.45 kJ/mol Relay (1.0) Calculated Property
Δfus 14.39 kJ/mol Joback Calculated Property
Δvap 76.63 kJ/mol Relay (1.0) Calculated Property
IE 8.01 eV Relay (1.0) Calculated Property
log10WS -2.46 Relay (1.0) Calculated Property
logPoct/wat 1.834 Crippen Calculated Property
McVol 134.370 ml/mol McGowan Calculated Property
Pc 3337.38 kPa Joback Calculated Property
Inp 1711.00 NIST
Tboil 589.20 K Relay (1.0) Calculated Property
Tc 812.88 K Relay (1.0) Calculated Property
Tfus 340.16 K Relay (1.0) Calculated Property
Vc 0.480 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [318.49; 391.80] J/mol×K [592.80; 836.85] Show Hide
Cp,gas 318.49 J/mol×K 592.80 Joback Calculated Property
Cp,gas 332.96 J/mol×K 633.48 Joback Calculated Property
Cp,gas 346.52 J/mol×K 674.15 Joback Calculated Property
Cp,gas 359.17 J/mol×K 714.83 Joback Calculated Property
Cp,gas 370.92 J/mol×K 755.50 Joback Calculated Property
Cp,gas 381.79 J/mol×K 796.18 Joback Calculated Property
Cp,gas 391.80 J/mol×K 836.85 Joback Calculated Property

Similar Compounds

2(1H)-Naphthalenone, 7-methoxy. 2(1H)-Naphthalenone, 1-methyl. 17«alpha»-ethynylestradiol, 3-acetate. 17«alpha»-ethynylestradiol, 3-propionate. Oestrone, 6-dehydro, TFA. Mestranol. 17«alpha»-ethynylestradiol, 3-butyrate. 2-[5-methoxy-2-methyl-1-(3-phenylprop-2-enoyl)indol-3-yl]acetic acid. 17«alpha»-ethynylestradiol, 3-formate. Estra-1,3,5(10),6-tetraene-3,17-diol, (17«beta»)-. Estriol, 3-(tert-butyldimethylsilyl) ether. Estradiol dipropionate. Estradiol dipropionate. Estradiol Benzoate. Benzquinamide M (O-des-Et), acetylated.

Find more compounds similar to 2(1H)-Naphthalenone, 6-methoxy.

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.