Chemical Properties of 2,6-Bis(picrylazo)-3,5-dinitropyridine

2,6-Bis(picrylazo)-3,5-dinitropyridine

InChI
InChI=1S/C17H5N13O16/c31-23(32)6-1-8(25(35)36)14(9(2-6)26(37)38)19-21-16-12(29(43)44)5-13(30(45)46)17(18-16)22-20-15-10(27(39)40)3-7(24(33)34)4-11(15)28(41)42/h1-5H/b21-19+,22-20+
InChI Key
BBVWILOPQSPUHG-UHFFFAOYSA-N
Formula
C17H5N13O16
SMILES
O=[N+]([O-])c1cc([N+](=O)[O-])c(/N=N/c2nc(/N=N/c3c([N+](=O)[O-])cc([N+](=O)[O-])cc3[N+](=O)[O-])c([N+](=O)[O-])cc2[N+](=O)[O-])c([N+](=O)[O-])c1
Molecular Weight1
647.30
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Physical Properties

Property Value Unit Source
Δcsolid -8021.60 ± 0.84 kJ/mol NIST
Δfgas 740.25 kJ/mol Relay (1.0) Calculated Property
Δfsolid 617.10 ± 5.00 kJ/mol NIST
Δvap 156.28 kJ/mol Relay (1.0) Calculated Property
IE 11.30 eV Relay (1.0) Calculated Property
log10WS -7.17 Relay (1.0) Calculated Property
logPoct/wat 5.178 Crippen Calculated Property
McVol 359.770 ml/mol McGowan Calculated Property
Tfus 555.00 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Standard Gibbs free energy of formation, Acentric Factor for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Similar Compounds

N-Stearoyldextramine. Nomifensine M(HO-methoxy), diacetylated. 17.alpha.-Ethynylestradiol, 3-(tert-butyldimethylsilyl) ether. pimaricin. propyl-«delta»1-tetrahydrocannabinolic acid, n-butyl-boronate. .delta.1-tetrahydrocannabinolic acid, n-butyl-boronate. Guanine deoxyriboside, TMS. Bialophos, N,O,O-tris(tert-butyldimethylsilyl)deriv.. Venlafaxine-M (O-desmethyl-HO-) isomer-2 2AC. 1-Methylhypoxanthine riboside, TMS. Nomifensine M(HO), diacetylated, isomer # 1. 2'-Deoxyadenosine, 3',5'-bis(O-TMTBSi). 2'-Deoxyadenosine, 3',5'-bis-O-cyclotetramethylene-isopropylsilyl. «delta»1-tetrahydrocannabinolic acid, methyl-boronate. Hypoxanthine riboside, TMS.

Find more compounds similar to 2,6-Bis(picrylazo)-3,5-dinitropyridine.

Sources

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