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Inherent Properties, Identifiers and References
ChemSpider ID: 4182808
Empirical Formula: C31H32N2O2
Molecular Weight: 464.598
Nominal Mass: 464 Da
Average Mass: 464.598 Da
Monoisotopic Mass: 464.246378 Da
Quick Links: Permalink Similar Isomers
Systematic Name: 1,3-dibenzyl-2-(4-benzyloxy-3-methoxy-phenyl)imidazolidine
SMILES: O(c1ccc(cc1OC)C3N(CCN3Cc2ccccc2)Cc4ccccc4)Cc5ccccc5
InChI: InChI=1/C31H32N2O2/c1-34-30-21-28(17-18-29(30)35-24-27-15-9-4-10-​16-27)31-32(22-25-11-5-2-6-12-25)19-20-33(31)23-26-13-7-3-8-14-26​/h2-18,21,31H,19-20,22-24H2,1H3
InChIKey: YEFWOMXEAPTURA-UHFFFAOYAM
Associated Data Sources and Commercial Suppliers
Names and Synonyms

Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts

1,3-diben​zyl-2-[4-​(benzylox​y)-3-meth​oxyphenyl​]imidazol​idine

Database ID(s)

Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts

(Details...) Predicted Properties
LogP: ACD/LogP: 5.50
XLogP: 6.30
# of Rule of 5 Violations: 1
ACD/LogD (pH 5.5): 5.09 ACD/LogD (pH 7.4): 5.49
ACD/BCF (pH 5.5): 3440.04 ACD/BCF (pH 7.4): 8693.21
ACD/KOC (pH 5.5): 9040.82 ACD/KOC (pH 7.4): 22846.79
#H bond acceptors: 4 #H bond donors: 0
#Freely Rotating Bonds: 9 Polar Surface Area: 24.94 Å2
Index of Refraction: 1.625 Molar Refractivity: 141.58 cm3
Molar Volume: 400.3 cm3 Polarizability: 56.13 10-24cm3
Surface Tension: 49.8 dyne/cm Density: 1.16 g/cm3
Flash Point: 152.2 °C Enthalpy of Vaporization: 86.58 kJ/mol
Boiling Point: 578.5 °C at 760 mmHg Vapour Pressure: 2.21E-13 mmHg at 25°C
            
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  5.54

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  575.51  (Adapted Stein & Brown method)
    Melting Pt (deg C):  247.87  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  1.21E-012  (Modified Grain method)
    Subcooled liquid VP: 3.2E-010 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):  0.2301
       log Kow used: 5.54 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  0.0068093 mg/L

 ECOSAR Class Program (ECOSAR v0.99h):
    Class(es) found:
       Aliphatic Amines

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   3.75E-013  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  3.215E-012 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  5.54  (KowWin est)
  Log Kaw used:  -10.814  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  16.354
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   0.7639
   Biowin2 (Non-Linear Model)     :   0.8652
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   1.6126  (recalcitrant)
   Biowin4 (Primary Survey Model) :   2.7703  (weeks       )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :  -0.4383
   Biowin6 (MITI Non-Linear Model):   0.0006
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -2.3293
 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):  4.27E-008 Pa (3.2E-010 mm Hg)
  Log Koa (Koawin est  ): 16.354
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  70.3 
       Octanol/air (Koa) model:  5.55E+003 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  1 
       Mackay model           :  1 
       Octanol/air (Koa) model:  1 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant = 335.6268 E-12 cm3/molecule-sec
      Half-Life =     0.032 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =    22.945 Min
   Ozone Reaction:
      No Ozone Reaction Estimation
   Fraction sorbed to airborne particulates (phi): 1 (Junge,Mackay)
    Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
      Koc    :  6.153E+007
      Log Koc:  7.789 

 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 = 3.562 (BCF = 3647)
       log Kow used: 5.54 (estimated)

 Volatilization from Water:
    Henry LC:  3.75E-013 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 3.365E+009  hours   (1.402E+008 days)
    Half-Life from Model Lake : 3.671E+010  hours   (1.53E+009 days)

 Removal In Wastewater Treatment:
    Total removal:              88.76  percent
    Total biodegradation:        0.75  percent
    Total sludge adsorption:    88.02  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       0.00147         0.765        1000       
   Water     2.13            4.32e+003    1000       
   Soil      66.3            8.64e+003    1000       
   Sediment  31.6            3.89e+004    0          
     Persistence Time: 9.69e+003 hr




        
Descriptors: 0, 0, 0, 0, 0, 0, 0, 5, 0, 0, 0, 0, 4, 18, 10, 0, 24, 0, 0, 1, 0, 0, 0, 0
CategoryTargetPDB CodeLASSO Score
Nuclear Hormone ReceptorsER, estrogen receptor; antagonist3ert0.73
Other EnzymesInhA, enoyl ACP reductase1p440.64
Other EnzymesHIVPR, HIV protease1hpx0.11
Nuclear Hormone ReceptorsPPARg, peroxisome proliferator activated receptor1fm90.07
Other EnzymesHIVRT, HIV reverse transcriptase1rt10.02
Nuclear Hormone ReceptorsRXRa, retinoic X receptor R1mvc0.02
KinasesVEGFr2, vascular endothelial growth factor receptor1vr20.02
Serine ProteasesFXa, factor Xa1f0r0.02
KinasesSRC, tyrosine kinase SRC2src0.01
Serine ProteasesThrombin1ba80.01
Other EnzymesHMGR, hydroxymethylglutaryl-CoA reductase1hw80.01
MetalloenzymesPDE5, phosphodiesterase 51xp00.01
Other EnzymesAChE, acetylcholinesterase1eve0.01
Nuclear Hormone ReceptorsMR, mineralocorticoid receptor2aa20.01
Nuclear Hormone ReceptorsPR, progesterone receptor1sr70.01
Other EnzymesPARP, poly(ADP-ribose) polymerase1efy0.01
KinasesPDGFrb, platelet derived growth factor receptor kinaseN/A0.00
Other EnzymesPNP, purine nucleoside phosphorylase1b8o0.00
Other EnzymesAmpC, AmpC beta-lactamase1xgj0.00
Folate EnzymesGART, glycinamide ribonucleotide transformylase1c2t0.00
Nuclear Hormone ReceptorsER, estrogen receptor; agonist1l2i0.00
Folate EnzymesDHFR, dihydrofolate reductase3dfr0.00
MetalloenzymesACE, angiotensin-converting enzyme1o860.00
Serine ProteasesTrypsin1bju0.00
Other EnzymesGPB, glycogen phosphorylase1a8i0.00
Other EnzymesSAHH, S-adenosyl-homocysteine hydrolase1a7a0.00
KinasesFGFr1, fibroblast growth factor receptor kinase1agw0.00
Other EnzymesCOX-2, cyclooxygenase-21cx20.00
KinasesEGFr, epidermal growth factor receptor1m170.00
Nuclear Hormone ReceptorsGR, glucocorticoid receptor1m2z0.00
Other EnzymesALR2, aldose reductase1ah30.00
Other EnzymesCOX-1, cyclooxygenase-11p4g0.00
Other EnzymesNA, neuraminidase1a4g0.00
KinasesTK, thymidine kinase1kim0.00
MetalloenzymesADA, adenosine deaminase1stw0.00
KinasesP38 MAP, P38 mitogen activated protein1kv20.00
MetalloenzymesCOMT, catechol O-methyltransferase1h1d0.00
Nuclear Hormone ReceptorsAR, androgen receptor1xq20.00
KinasesHSP90, human heat shock protein 901uy60.00
KinasesCDK2, cyclindependent kinase 21ckp0.00