Chemical Properties of Purine, 2-amino-6-propoxy- (CAS 6331-91-5)

Purine, 2-amino-6-propoxy-

InChI
InChI=1S/C8H11N5O/c1-2-3-14-7-5-6(11-4-10-5)12-8(9)13-7/h4H,2-3H2,1H3,(H3,9,10,11,12,13)
InChI Key
WWMYHQCOEFJVFT-UHFFFAOYSA-N
Formula
C8H11N5O
SMILES
CCCOc1nc(N)nc2nc[nH]c12
Molecular Weight1
193.21
CAS
6331-91-5
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Physical Properties

Property Value Unit Source
ω 0.6912 Relay (1.0) Calculated Property
Δf 309.59 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas -12.73 kJ/mol Relay (1.0) Calculated Property
Δvap 101.22 kJ/mol Relay (1.0) Calculated Property
IE 8.47 eV Relay (1.0) Calculated Property
log10WS -3.47 Relay (1.0) Calculated Property
logPoct/wat 0.242 Crippen Calculated Property
McVol 140.430 ml/mol McGowan Calculated Property
Pc 3947.63 kPa Relay (1.0-beta) Calculated Property
Tboil 609.02 K Relay (1.0) Calculated Property
Tc 911.94 K Relay (1.0) Calculated Property
Tfus 457.35 K Relay (1.0) Calculated Property
Vc 0.540 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

Purine, 2-amino-6-butoxy-. Purine, 2-amino-6-ethoxy-. Purine, 6-propoxy-. Purine, 6-ethoxy-. 9H-purine-6(1h)-thione, 1-methyl-9-beta-d-ribofuranosyl-. Guanosine. Guanosine. Adenosine, 2-azido-. Adenosine, 2-methoxy-. Tetrazepam M (hydroxy-), isomer 2, hydrolysis, acetylated. Mirtazapine-M (HO-) AC. Mirtazapine-M (nor-HO-) 2AC. Mirtazapine-M (nor-HO-methoxy-) 2AC. famotidine. Guanosine, 2'-deoxy-.

Find more compounds similar to Purine, 2-amino-6-propoxy-.

Sources

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