Chemical Properties of 2-Thiophenine, 3,5-dinitro-n-phenyl thiophene, 2-anilino-3,5-dinitro- (CAS 959-38-6)

2-Thiophenine, 3,5-dinitro-n-phenyl thiophene, 2-anilino-3,5-dinitro-

InChI
InChI=1S/C10H7N3O4S/c14-12(15)8-6-9(13(16)17)18-10(8)11-7-4-2-1-3-5-7/h1-6,11H
InChI Key
XTHINSIFAJZOSG-UHFFFAOYSA-N
Formula
C10H7N3O4S
SMILES
O=[N+]([O-])c1cc([N+](=O)[O-])c(Nc2ccccc2)s1
Molecular Weight1
265.25
CAS
959-38-6
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 0.7189 Relay (1.0) Calculated Property
ΔfG° 358.01 kJ/mol Relay (1.0-beta) Calculated Property
ΔfH°gas 202.95 kJ/mol Relay (1.0) Calculated Property
ΔvapH° 96.93 kJ/mol Relay (1.0) Calculated Property
IE 8.05 eV Relay (1.0) Calculated Property
log10WS -4.63 Relay (1.0) Calculated Property
logPoct/wat 3.308 Crippen Calculated Property
McVol 169.710 ml/mol McGowan Calculated Property
Pc 5131.43 kPa Relay (1.0-beta) Calculated Property
Tboil 619.97 K Relay (1.0) Calculated Property
Tc 990.06 K Relay (1.0) Calculated Property
Tfus 434.62 K Relay (1.0) Calculated Property
Vc 0.577 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

«delta»1-tetrahydrocannabinolic acid, phenyl-boronate. 1-Oxo-2-(3-phenylrhodanin-5-ylidene)-3-pyridinium-4-naphthoxide. Lysergol. Guanine deoxyriboside, TMS. Cytidine, etho-oxime-TMS derivative. N6-(cyclotetramethylene-tertbutylsilyl)-2'-Deoxyadenosine, 3',5'-bis-O-TBDMS. Vobassan-17-oic acid, 4-demethyl-3-oxo-, methyl ester. Tazettine. Hydrocodone. 9H-Purin-2-amine, N-(trimethylsilyl)-6-[(trimethylsilyl)oxy]-9-[2,3,5-tris-O-(trimethylsilyl)-«beta»-D-ribofuranosyl]-. Cytidine, metho-oxime-TMS derivative. Retroisosenine. 5-Pregnen-3-«beta»-ol, 20-«alpha»-GlcNAc, MeTMS. Hydromorphone. 5-Pregnen-3-«alpha»,20-«alpha»-diol-20-GlcNAc TMS.

Find more compounds similar to 2-Thiophenine, 3,5-dinitro-n-phenyl thiophene, 2-anilino-3,5-dinitro-.

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.