N-[5-(4-Fluorophenyl)-1,3,4-thiadiazol-2-yl]-N-methylpropanamide
Fc1ccc(cc1)c2nnc(s2)N(C(=O)CC)C CopyCopied
InChI=1S/C12H12FN3OS/c1-3-10(17)16(2)12-15-14-11(18-12)8-4-6-9(13)7-5-8/h4-7H,3H2,1-2H3 CopyCopied
DCCGEGCLBQDHQA-UHFFFAOYSA-N CopyCopied
Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts
N-[5-(4-Fluoro-phenyl)-[1,3,4]thiadiazol-2-yl]-N-methyl-propionamide
ASN 05668587 [DBID]
ZINC01356310 [DBID]
Predicted data is generated using the ACD/Labs’ ACD/PhysChem Suite, for more information see their website.
Predicted data is generated using the US Environmental Protection Agency’s EPISuite, for more information see their website.
Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 estimate) = 2.25 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42): Boiling Pt (deg C): 427.14 (Adapted Stein & Brown method) Melting Pt (deg C): 178.57 (Mean or Weighted MP) VP(mm Hg,25 deg C): 4.57E-008 (Modified Grain method) Subcooled liquid VP: 1.8E-006 mm Hg (25 deg C, Mod-Grain method) Water Solubility Estimate from Log Kow (WSKOW v1.41): Water Solubility at 25 deg C (mg/L): 231.7 log Kow used: 2.25 (estimated) no-melting pt equation used Water Sol Estimate from Fragments: Wat Sol (v1.01 est) = 878.95 mg/L ECOSAR Class Program (ECOSAR v0.99h): Class(es) found: Neutral Organics Henrys Law Constant (25 deg C) [HENRYWIN v3.10]: Bond Method : 4.35E-012 atm-m3/mole Group Method: Incomplete Henrys LC [VP/WSol estimate using EPI values]: 6.885E-011 atm-m3/mole Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]: Log Kow used: 2.25 (KowWin est) Log Kaw used: -9.750 (HenryWin est) Log Koa (KOAWIN v1.10 estimate): 12.000 Log Koa (experimental database): None Probability of Rapid Biodegradation (BIOWIN v4.10): Biowin1 (Linear Model) : 0.0214 Biowin2 (Non-Linear Model) : 0.0002 Expert Survey Biodegradation Results: Biowin3 (Ultimate Survey Model): 2.1517 (months ) Biowin4 (Primary Survey Model) : 3.6839 (days-weeks ) MITI Biodegradation Probability: Biowin5 (MITI Linear Model) : 0.1500 Biowin6 (MITI Non-Linear Model): 0.0007 Anaerobic Biodegradation Probability: Biowin7 (Anaerobic Linear Model): -0.2467 Ready Biodegradability Prediction: NO Hydrocarbon Biodegradation (BioHCwin v1.01): Structure incompatible with current estimation method! Sorption to aerosols (25 Dec C)[AEROWIN v1.00]: Vapor pressure (liquid/subcooled): 0.00024 Pa (1.8E-006 mm Hg) Log Koa (Koawin est ): 12.000 Kp (particle/gas partition coef. (m3/ug)): Mackay model : 0.0125 Octanol/air (Koa) model: 0.245 Fraction sorbed to airborne particulates (phi): Junge-Pankow model : 0.311 Mackay model : 0.5 Octanol/air (Koa) model: 0.952 Atmospheric Oxidation (25 deg C) [AopWin v1.92]: Hydroxyl Radicals Reaction: OVERALL OH Rate Constant = 4.2334 E-12 cm3/molecule-sec Half-Life = 2.527 Days (12-hr day; 1.5E6 OH/cm3) Half-Life = 30.319 Hrs Ozone Reaction: No Ozone Reaction Estimation Fraction sorbed to airborne particulates (phi): 0.406 (Junge,Mackay) Note: the sorbed fraction may be resistant to atmospheric oxidation Soil Adsorption Coefficient (PCKOCWIN v1.66): Koc : 335.7 Log Koc: 2.526 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]: Rate constants can NOT be estimated for this structure! Bioaccumulation Estimates from Log Kow (BCFWIN v2.17): Log BCF from regression-based method = 1.034 (BCF = 10.82) log Kow used: 2.25 (estimated) Volatilization from Water: Henry LC: 4.35E-012 atm-m3/mole (estimated by Bond SAR Method) Half-Life from Model River: 2.192E+008 hours (9.135E+006 days) Half-Life from Model Lake : 2.392E+009 hours (9.965E+007 days) Removal In Wastewater Treatment: Total removal: 2.55 percent Total biodegradation: 0.10 percent Total sludge adsorption: 2.46 percent Total to Air: 0.00 percent (using 10000 hr Bio P,A,S) Level III Fugacity Model: Mass Amount Half-Life Emissions (percent) (hr) (kg/hr) Air 4.43e-005 60.6 1000 Water 18.3 1.44e+003 1000 Soil 81.6 2.88e+003 1000 Sediment 0.102 1.3e+004 0 Persistence Time: 2.14e+003 hr
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