Chemical Properties of 6-HYDROXY-1,3-BENZOTHIAZOLE-2-SULFONAMIDE

6-HYDROXY-1,3-BENZOTHIAZOLE-2-SULFONAMIDE

InChI
InChI=1S/C7H6N2O3S2/c8-14(11,12)7-9-5-2-1-4(10)3-6(5)13-7/h1-3,10H,(H2,8,11,12)
InChI Key
NOOBQTYVTDBXTL-UHFFFAOYSA-N
Formula
C7H6N2O3S2
SMILES
NS(=O)(=O)c1nc2ccc(O)cc2s1
Molecular Weight1
230.27
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Physical Properties

Property Value Unit Source
ω 0.7544 Relay (1.0) Calculated Property
ΔfG° -114.84 kJ/mol Relay (1.0-beta) Calculated Property
ΔfH°gas -263.03 kJ/mol Relay (1.0) Calculated Property
ΔvapH° 109.70 kJ/mol Relay (1.0) Calculated Property
IE 8.50 eV Relay (1.0) Calculated Property
log10WS -2.50 Aq. Solubility Prediction
logPoct/wat 0.649 Crippen Calculated Property
McVol 140.840 ml/mol McGowan Calculated Property
Pc 5282.75 kPa Relay (1.0-beta) Calculated Property
Tboil 640.89 K Relay (1.0) Calculated Property
Tc 1000.54 K Relay (1.0) Calculated Property
Tfus 523.54 K Relay (1.0) Calculated Property
Vc 0.496 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

Ethoxzolamide. 1,3-benzothiazole-2-sulfonamide. N-(2-sulfamoyl-1,3-benzothiazol-6-yl)acetamide. 2(3H)-Benzothiazolethione, 6-ethoxy-. N-cyclohexyl-2-benzothiazole sulfonamide. 2-Hydroxy-2-phenylethylamine, ferrocenylboronate. 9,10-Dihydrophenanthrene-cis-9,10-diol, ferrocenylboronate. Poligodial + p-Tyr (ethyl ester) adduct (S), acetylated, # 1. 6-Tetrahydrocannabinol, 7-hydroxy, allyl-DMS. Poligodial + p-Tyr (ethyl ester) adduct (S). N-Acetylnornarcotine. Glyceofuran, TMS. 2(1H)-Pyrimidinone, 1-[2,3-bis-O-(trimethylsilyl)-«beta»-D-ribofuranosyl]-4-(trimethylsiloxy)-, 5'-[bis(trimethylsilyl) phosphate]. Poligodial + o-Tyr (ethyl ester) adduct (R,S). Poligodial + p-Tyr (ethyl ester) adduct (S), acetylated, # 2.

Find more compounds similar to 6-HYDROXY-1,3-BENZOTHIAZOLE-2-SULFONAMIDE.

Sources

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