Chemical Properties of Purine, 6-propoxy- (CAS 5417-86-7)

Purine, 6-propoxy-

InChI
InChI=1S/C8H10N4O/c1-2-3-13-8-6-7(10-4-9-6)11-5-12-8/h4-5H,2-3H2,1H3,(H,9,10,11,12)
InChI Key
UQQKEKTYLCCYSN-UHFFFAOYSA-N
Formula
C8H10N4O
SMILES
CCCOc1ncnc2nc[nH]c12
Molecular Weight1
178.19
CAS
5417-86-7
Other Names
  • 6-propoxy-1H-purine
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Physical Properties

Property Value Unit Source
ω 0.5821 Relay (1.0) Calculated Property
Δf 243.59 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas 32.01 kJ/mol Relay (1.0) Calculated Property
Δvap 75.78 kJ/mol Relay (1.0) Calculated Property
IE 8.84 eV Relay (1.0) Calculated Property
log10WS -2.86 Relay (1.0) Calculated Property
logPoct/wat 0.660 Crippen Calculated Property
McVol 130.450 ml/mol McGowan Calculated Property
Pc 4358.89 kPa Relay (1.0-beta) Calculated Property
Tboil 589.37 K Relay (1.0) Calculated Property
Tc 859.64 K Relay (1.0) Calculated Property
Tfus 421.96 K Relay (1.0) Calculated Property
Vc 0.509 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

Purine, 6-ethoxy-. Purine, 2-amino-6-propoxy-. Purine, 2-amino-6-butoxy-. Purine, 2-amino-6-ethoxy-. Purine, 6-(2,2,2-trifluoroethoxy)-. famotidine. Hypoxanthine deoxyriboside, TMS. Tetrazepam M (hydroxy-), isomer 1, hydrolysis, acetylated. Sertraline, acetyl. Sertraline, nor, acetyl. Glyburide. Cytidine, 2',3',5'-tris(trimethylsilyl) ether. Inosine. Tetrazepam M (hydroxy-), isomer 2, hydrolysis, acetylated. Thioinosine.

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

Sources

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