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6-chloro-N,N-di(prop-2-en-1-yl)-N'-propyl-1,3,5-triazine-2,4-diamine

10548992 (ChemSpider ID)
C₁₂H₁₈ClN₅
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Mass

Molecular weight:	267.7578
Nominal mass:	267 Da
Average mass:	267.7578 Da
Monoisotopic mass:	267.125073 Da

Machine readable identifiers

Systematic name:

6-chloro-N,N-di(prop-2-en-1-yl)-N'-propyl-1,3,5-triazine-2,4-diamine

SMILES:

Clc1nc(NCCC)nc(n1)N(CC=C)CC=C Copied

InChI:

InChI=1/C12H18ClN5/c1-4-7-14-11-15-10(13)16-12(17-11)18(8-5-2)9-6-3/h5-6H,2-4,7-9H2,1H3,(H,14,15,16,17) Copied

InChIKey:

WWJQEAYTFXWZOB-UHFFFAOYAB

Std. InChI:

InChI=1S/C12H18ClN5/c1-4-7-14-11-15-10(13)16-12(17-11)18(8-5-2)9-6-3/h5-6H,2-4,7-9H2,1H3,(H,14,15,16,17) Copied

Std. InChIKey:

WWJQEAYTFXWZOB-UHFFFAOYSA-N

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Publication or Magazine Article	Web-based Article (blog or commentary)
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Ligand/binding/crystal Structure Databases	Metabolic Pathways
Molecular Libraries Screening Center Network	Natural Products
NIH Substance Repository	Physical Properties (including SAR/QSAR databases)
Protein 3D Structures	Spectroscopy Databases
Substance Vendors	Theoretical Properties
Toxicology/Environmental Databases	Virtual Library

Patents

ACD/LogP:	4.59	# of Rule of 5 Violations:	0
ACD/LogD (pH 5.5):	5	ACD/LogD (pH 7.4):	5
ACD/BCF (pH 5.5):	1839	ACD/BCF (pH 7.4):	1841
ACD/KOC (pH 5.5):	7554	ACD/KOC (pH 7.4):	7562
#H bond acceptors:	5	#H bond donors:	1
#Freely Rotating Bonds:	7	Polar Surface Area:	53.94 Å²
Index of Refraction:	1.588	Molar Refractivity:	76.593 cm³
Molar Volume:	227.73 cm³	Polarizability:	30.364 10^-24cm³
Surface Tension:	49.227 dyne/cm	Density:	1.176 g/cm³
Flash Point:	203.784 °C	Enthalpy of Vaporization:	66.611 kJ/mol
Boiling Point:	413.346 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

                    
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  4.64

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  357.17  (Adapted Stein & Brown method)
    Melting Pt (deg C):  141.80  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  5.88E-006  (Modified Grain method)
    Subcooled liquid VP: 8.92E-005 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):  2.055
       log Kow used: 4.64 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  0.417 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   1.19E-007  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  1.008E-006 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  4.64  (KowWin est)
  Log Kaw used:  -5.313  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  9.953
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   0.0082
   Biowin2 (Non-Linear Model)     :   0.0000
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   1.7652  (months      )
   Biowin4 (Primary Survey Model) :   2.8422  (weeks       )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :   0.0312
   Biowin6 (MITI Non-Linear Model):   0.0000
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -1.4139
 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):  0.0119 Pa (8.92E-005 mm Hg)
  Log Koa (Koawin est  ): 9.953
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  0.000252 
       Octanol/air (Koa) model:  0.0022 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  0.00903 
       Mackay model           :  0.0198 
       Octanol/air (Koa) model:  0.15 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant =  82.0901 E-12 cm3/molecule-sec
      Half-Life =     0.130 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =     1.564 Hrs
   Ozone Reaction:
      OVERALL Ozone Rate Constant =     2.400000 E-17 cm3/molecule-sec
      Half-Life =     0.477 Days (at 7E11 mol/cm3)
      Half-Life =     11.460 Hrs
   Fraction sorbed to airborne particulates (phi): 0.0144 (Junge,Mackay)
    Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
      Koc    :  2244
      Log Koc:  3.351 

 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 = 2.552 (BCF = 356.3)
       log Kow used: 4.64 (estimated)

 Volatilization from Water:
    Henry LC:  1.19E-007 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River:       8052  hours   (335.5 days)
    Half-Life from Model Lake : 8.798E+004  hours   (3666 days)

 Removal In Wastewater Treatment:
    Total removal:              63.14  percent
    Total biodegradation:        0.57  percent
    Total sludge adsorption:    62.57  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       0.0538          2.46         1000       
   Water     10.8            1.44e+003    1000       
   Soil      74.4            2.88e+003    1000       
   Sediment  14.7            1.3e+004     0          
     Persistence Time: 1.97e+003 hr

Calculate properties at chemicalize.org

Category	Target	PDB Code	LASSO Score
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.98
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.83
Kinases	SRC, tyrosine kinase SRC	2src	0.81
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.60
Other Enzymes	ALR2, aldose reductase	1ah3	0.23
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.03
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.02
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.02
Other Enzymes	AmpC, AmpC beta-lactamase	1xgj	0.02
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Other Enzymes	HIVPR, HIV protease	1hpx	0.01
Kinases	HSP90, human heat shock protein 90	1uy6	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.01
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.00
Other Enzymes	PNP, purine nucleoside phosphorylase	1b8o	0.00
Folate Enzymes	DHFR, dihydrofolate reductase	3dfr	0.00
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; agonist	1l2i	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.00
Serine Proteases	Thrombin	1ba8	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00

6-chloro-N,N-di(prop-2-en-1-yl)-N'-propyl-1,3,5-triazine-2,4-diamine

Systematic name:

SMILES:

InChI:

InChIKey:

Std. InChI:

Std. InChIKey:

Associated Data Sources and Commercial Suppliers

Patents

Properties

Pharmacological Links

SimBioSys LASSO

6-chloro-N,N-di(prop-2-en-1-yl​)-N'-propyl-1,3,5-triazine-2,4​-diamine

Systematic name:

SMILES:

InChI:

InChIKey:

Std. InChI:

Std. InChIKey:

Associated Data Sources and Commercial Suppliers

Patents

Properties

Pharmacological Links

SimBioSys LASSO

6-chloro-N,N-di(prop-2-en-1-yl)-N'-propyl-1,3,5-triazine-2,4-diamine