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Search term: 6-geranylgeranyl-2-methylbenzene-1,4-diol (Found by synonym)

ChemSpider 2D Image | 2-(geranylgeranyl)-methyl-benzohydroquin | C27H40O2

2-(geranylgeranyl)-methyl-benzohydroquin

  • Molecular FormulaC27H40O2
  • Average mass396.605 Da
  • Monoisotopic mass396.302826 Da
  • ChemSpider ID10470958
  • Double-bond stereo - Double-bond stereo


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

1,4-Benzenediol, 2-methyl-6-[(2E,6E,10E)-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraen-1-yl]- [ACD/Index Name]
2-(geranylgeranyl)-methyl-benzohydroquin
2-Methyl-6-[(2E,6E,10E)-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraen-1-yl]-1,4-benzenediol [ACD/IUPAC Name]
2-Méthyl-6-[(2E,6E,10E)-3,7,11,15-tétraméthyl-2,6,10,14-hexadécatétraén-1-yl]-1,4-benzènediol [French] [ACD/IUPAC Name]
2-Methyl-6-[(2E,6E,10E)-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraen-1-yl]-1,4-benzoldiol [German] [ACD/IUPAC Name]
2-methyl-6-geranylgeranyl-1,4-benzoquinol
57576-81-5 [RN]
2-methyl-6-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]benzene-1,4-diol
6-geranylgeranyl-2-methylbenzene-1,4-diol
C20737
  • Miscellaneous
    • Chemical Class:

      A polyprenylhydroquinone that is 2-methylbenzene-1,4-diol substituted by a geranylgeranyl group at position 6. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:75411, CHEBI:75411
    • Compound Source:

      Ananas comosus PlantCyc CPD-11712
      Aquilegia coerulea PlantCyc CPD-11712
      Arabidopsis thaliana col PlantCyc CPD-11712
      Asparagus officinalis PlantCyc CPD-11712
      Brachypodium distachyon PlantCyc CPD-11712
      Camptotheca acuminata PlantCyc CPD-11712
      Carica papaya PlantCyc CPD-11712
      Chenopodium quinoa PlantCyc CPD-11712
      Chlamydomonas reinhardtii PlantCyc CPD-11712
      Citrus clementina PlantCyc CPD-11712
      Citrus sinensis PlantCyc CPD-11712
      Daucus carota subsp. sativus PlantCyc CPD-11712
      Dioscorea rotundata PlantCyc CPD-11712
      Fragaria vesca subsp. vesca PlantCyc CPD-11712
      Hordeum vulgare subsp. vulgare PlantCyc CPD-11712
      Kalanchoe fedtschenkoi PlantCyc CPD-11712
      Leersia perrieri PlantCyc CPD-11712
      Linum usitatissimum PlantCyc CPD-11712
      Manihot esculenta PlantCyc CPD-11712
      Miscanthus sinensis PlantCyc CPD-11712
      Musa acuminata PlantCyc CPD-11712
      Nicotiana tabacum PlantCyc CPD-11712
      Oropetium thomaeum PlantCyc CPD-11712
      Oryza brachyantha PlantCyc CPD-11712
      Oryza glaberrima PlantCyc CPD-11712
      Oryza punctata PlantCyc CPD-11712
      Oryza rufipogon PlantCyc CPD-11712
      Oryza sativa Japonica Group PlantCyc CPD-11712
      Panicum hallii PlantCyc CPD-11712
      Panicum virgatum PlantCyc CPD-11712
      Petunia axillaris PlantCyc CPD-11712
      Populus trichocarpa PlantCyc CPD-11712
      Prunus persica PlantCyc CPD-11712
      Rosa chinensis PlantCyc CPD-11712
      Setaria italica PlantCyc CPD-11712
      Setaria viridis PlantCyc CPD-11712
      Solanum lycopersicum PlantCyc CPD-11712
      Solanum pennellii PlantCyc CPD-11712
      Sorghum bicolor PlantCyc CPD-11712
      Spinacia oleracea PlantCyc CPD-11712
      Triticum aestivum PlantCyc CPD-11712
      Triticum urartu PlantCyc CPD-11712
      vitamin E biosynthesis (tocotrienols) PlantCyc CPD-11712
      Vitis vinifera PlantCyc CPD-11712
      Zea mays subsp. mays PlantCyc CPD-11712
    • Bio Activity:

      2-methyl-6-geranylgeranyl-1,4-benzoquinol -> delta-tocotrienol PlantCyc CPD-11712
      delta-tocotrienol <- 2-methyl-6-geranylgeranyl-1,4-benzoquinol + 2-methyl-6-geranylgeranyl-1,4-benzoquinol PlantCyc CPD-11712
      geranylgeranyl diphosphate + homogentisate + H+ -> 2-methyl-6-geranylgeranyl-1,4-benzoquinol + CO2 + diphosphate PlantCyc CPD-11712
      homogentisate + geranylgeranyl diphosphate + geranylgeranyl diphosphate + homogentisate + H+ + H+ -> CO2 + 2-methyl-6-geranylgeranyl-1,4-benzoquinol + 2-methyl-6-geranylgeranyl-1,4-benzoquinol + CO2 + diphosphate + diphosphate PlantCyc CPD-11712
      S-adenosyl-L-methionine + 2-methyl-6-geranylgeranyl-1,4-benzoquinol -> S-adenosyl-L-homocysteine + 2,3-dimethyl-6-geranylgeranyl-1,4-benzoquinol + H+ PlantCyc CPD-11712
      S-adenosyl-L-methionine + 2-methyl-6-geranylgeranyl-1,4-benzoquinol + 2-methyl-6-geranylgeranyl-1,4-benzoquinol -> S-adenosyl-L-homocysteine + S-adenosyl-L-homocysteine + 2,3-dimethyl-6-geranylgeranyl-1,4-benzoquinol + H+ + H+ PlantCyc CPD-11712

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

Density: 1.0±0.1 g/cm3
Boiling Point: 545.2±38.0 °C at 760 mmHg
Vapour Pressure: 0.0±1.5 mmHg at 25°C
Enthalpy of Vaporization: 85.5±3.0 kJ/mol
Flash Point: 228.6±21.4 °C
Index of Refraction: 1.540
Molar Refractivity: 127.4±0.3 cm3
#H bond acceptors: 2
#H bond donors: 2
#Freely Rotating Bonds: 11
#Rule of 5 Violations: 1
ACD/LogP: 9.30
ACD/LogD (pH 5.5): 8.58
ACD/BCF (pH 5.5): 1000000.00
ACD/KOC (pH 5.5): 1103486.50
ACD/LogD (pH 7.4): 8.58
ACD/BCF (pH 7.4): 1000000.00
ACD/KOC (pH 7.4): 1102854.25
Polar Surface Area: 40 Å2
Polarizability: 50.5±0.5 10-24cm3
Surface Tension: 36.9±3.0 dyne/cm
Molar Volume: 406.2±3.0 cm3

Predicted data is generated using the US Environmental Protection Agency�s EPISuite™

                        
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  10.82

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  501.47  (Adapted Stein & Brown method)
    Melting Pt (deg C):  204.74  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  6.59E-012  (Modified Grain method)
    Subcooled liquid VP: 5.26E-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):  6.986e-006
       log Kow used: 10.82 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  0.0010869 mg/L

 ECOSAR Class Program (ECOSAR v0.99h):
    Class(es) found:
       Phenols
       Quinone/Hydroquinone

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   1.80E-008  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  4.923E-007 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  10.82  (KowWin est)
  Log Kaw used:  -6.133  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  16.953
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   0.8997
   Biowin2 (Non-Linear Model)     :   0.5862
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   2.2858  (weeks-months)
   Biowin4 (Primary Survey Model) :   3.2178  (weeks       )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :  -0.0138
   Biowin6 (MITI Non-Linear Model):   0.0087
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -0.2229
 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):  7.01E-008 Pa (5.26E-010 mm Hg)
  Log Koa (Koawin est  ): 16.953
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  42.8 
       Octanol/air (Koa) model:  2.2E+004 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  0.999 
       Mackay model           :  1 
       Octanol/air (Koa) model:  1 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant = 505.3561 E-12 cm3/molecule-sec
      Half-Life =     0.021 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =    15.239 Min
   Ozone Reaction:
      OVERALL Ozone Rate Constant =   172.000000 E-17 cm3/molecule-sec
      Half-Life =     0.007 Days (at 7E11 mol/cm3)
      Half-Life =      9.594 Min
   Reaction With Nitrate Radicals May Be Important!
   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    :  7.936E+007
      Log Koc:  7.900 

 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 = 0.500 (BCF = 3.162)
       log Kow used: 10.82 (estimated)

 Volatilization from Water:
    Henry LC:  1.8E-008 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 6.478E+004  hours   (2699 days)
    Half-Life from Model Lake : 7.069E+005  hours   (2.945E+004 days)

 Removal In Wastewater Treatment:
    Total removal:              94.04  percent
    Total biodegradation:        0.78  percent
    Total sludge adsorption:    93.26  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       0.00187         0.122        1000       
   Water     1.9             900          1000       
   Soil      28.1            1.8e+003     1000       
   Sediment  70              8.1e+003     0          
     Persistence Time: 3.1e+003 hr




                    

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