Chemical Properties of Trichlormethiazide

Trichlormethiazide

InChI
InChI=1S/C8H8Cl3N3O4S2/c9-3-1-4-6(2-5(3)19(12,15)16)20(17,18)14-8(13-4)7(10)11/h1-2,7-8,13-14H,(H2,12,15,16)
InChI Key
LMJSLTNSBFUCMU-UHFFFAOYSA-N
Formula
C8H8Cl3N3O4S2
SMILES
NS(=O)(=O)c1cc2c(cc1Cl)NC(C(Cl)Cl)NS2(=O)=O
Molecular Weight1
380.66
Other Names
  • 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-3-(dichloromethyl)-3,4-dihydro-, 1,1-dioxide
  • 3-(Dichloromethyl)-6-chloro-7-sulfamoyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide
  • 3-Dichloromethyl-6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide
  • 3-Dichloromethylhydrochlorothiazide
  • 6-Chloro-3-(dichloromethyl)-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
  • 6-Chloro-3-(dichloromethyl)-3,4-dihydro-2H-1,2,4-thiadiazine-7-sulfonamide 1,1-dioxide
  • 6-Chloro-3-(dichloromethyl)3,4-dihydro-7-sulfamoyl-1,2,4-benzothiadiazine-1,1-dioxide
  • 6-Chloro-3-(dichloromethyl)3,4-dihydro-7-sulfamyl-1,2,4-benzothiadiazine-1,1-dioxide
  • Achletin
  • Anatran
  • Anistadin
  • Aponorin
  • Carvacron
  • Chlopolidine
  • Ciba 7057-Su
  • Cretonin
  • Diu-Hydrin
  • Diurazida
  • Diurese
  • Diuroral
  • Esmarin
  • Eurinol
  • Fluitran
  • Flurese
  • Flutra
  • Gangesol
  • Hydrotrichlorothiazide
  • Intromene
  • Isestran
  • Kubacron
  • Metahydrin
  • Metatensin
  • NSC 61560
  • Nakva
  • Naqua
  • Naquasone
  • Naquival
  • Salurin
  • Schebitran
  • Tachionin
  • Tolcasone
  • Trichlormetazid
  • Trichlormethiazid
  • Trichloromethiadiazide
  • Trichloromethiazide
  • Triclordiuride
  • Triclormetiazide
  • Triflumen
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Physical Properties

Property Value Unit Source
Δfus 61.11 kJ/mol Joback Calculated Property
log10WS -2.68 Estimated Solubility
logPoct/wat 0.821 Crippen Calculated Property
McVol 211.800 ml/mol McGowan Calculated Property
Tfus 515.98 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy 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.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [512.04; 550.71] J/mol×K [791.36; 1034.39] Show Hide
Cp,gas 512.04 J/mol×K 791.36 Joback Calculated Property
Cp,gas 521.50 J/mol×K 831.86 Joback Calculated Property
Cp,gas 529.76 J/mol×K 872.37 Joback Calculated Property
Cp,gas 536.81 J/mol×K 912.87 Joback Calculated Property
Cp,gas 542.66 J/mol×K 953.38 Joback Calculated Property
Cp,gas 547.30 J/mol×K 993.88 Joback Calculated Property
Cp,gas 550.71 J/mol×K 1034.39 Joback Calculated Property

Similar Compounds

Polythiazide. CYCLOTHIAZIDE. Benzylmorphine. TCN. Nicocodine. Prajmaline. Morphinan-3,6-diol, 7,8-didehydro-4,5-epoxy-17-methyl- (5«alpha»,6«alpha»)-, bis(trifluoroacetate) (ester). BUPRENORPHINE. 6-O,N-Diacetylnorcodeine. Ethylmorphine. Norcodeine. QUINIDINE, M(HO-), AC. DIHYDROERGOTAMINE. Triazolo[4,5-d]pyrimidin-7-ol,3h-v-, 5-amino-3-(2',3'-o-isopropylidene-beta-d-ribofuranosyl)-, 5'-diphenyl phosphate (keto form). [2,2'-Bimorphinan]-3,3',6,6'-tetrol, 7,7',8,8'-tetradehydro-4,5:4',5'-diepoxy-17,17'-dimethyl-, (5«alpha»,6«alpha»)-(5'«alpha»,6'«alpha»)-.

Find more compounds similar to Trichlormethiazide.

Sources

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