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Ethyl 2-amino-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate

ChemSpider ID: 60975
Molecular Formula: C₇H₇F₃N₂O₂S
Average mass: 240.202896 Da
Monoisotopic mass: 240.018036 Da
Systematic name

Ethyl 2-amino-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate
SMILES and InChIs

SMILES:

FC(F)(F)c1nc(sc1C(=O)OCC)N Copied

Std. InChI:

InChI=1S/C7H7F3N2O2S/c1-2-14-5(13)3-4(7(8,9)10)12-6(11)15-3/h2H2,1H3,(H2,11,12) Copied

Std. InChIKey:

XJRPTMORGOIMMI-UHFFFAOYSA-N Copied
Cite this record
CSID:60975, http://www.chemspider.com/Chemical-Structure.60975.html (accessed 06:27, Jun 19, 2013) Copied

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

5-Thiazolecarboxylic acid, 2-amino-4-(trifluoromethyl)-, ethyl ester

Ethyl 2-amino-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate [ACD/IUPAC Name]

2-Amino-4-(4-tert-butylphenyl)thiophene-3-carboxamide

2-Amino-4-(trifluoromethyl)-5-(carbethoxy)thiazole

2-Amino-4-(trifluoromethyl)-5-thiazolecarboxylic acid ethyl ester

2-AMINO-4-TRIFLUOROMETHYL-THIAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

344-72-9 [RN]

5-Thiazolecarboxylic acid, 2-amino-4- (trifluoromethyl)-, ethyl ester

5-Thiazolecarboxylic acid, 2-amino-4-(trifluorom

5-Thiazolecarboxylic acid,2-amino-4-(trifluoromethyl)-, ethyl ester

More...

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

AI3-18593 [DBID]

AIDS073076 [DBID]

AIDS-073076 [DBID]

BRN 4810691 [DBID]

Maybridge3_003032 [DBID]

MFCD00153147 [DBID]

NSC 4465 [DBID]

NSC4465 [DBID]

ZINC01036886 [DBID]

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Properties

Experimental data
Predicted - ACD/Labs
Predicted - EPISuite
Predicted - ChemAxon

Data supplied by datasources and users.

Experimental Physico-chemical Properties

Experimental Melting Point:

170-172 °C SynQuest

170-172 °C SynQuest 8H70-3-24

Experimental LogP:

1.861 Vitas-M STK400047

Predicted data is generated using the ACD/Labs’ ACD/PhysChem Suite, for more information see their website.

ACD/LogP:	0.242	# of Rule of 5 Violations:	0
ACD/LogD (pH 5.5):	0.24	ACD/LogD (pH 7.4):	0.24
ACD/BCF (pH 5.5):	1.00	ACD/BCF (pH 7.4):	1.00
ACD/KOC (pH 5.5):	32.25	ACD/KOC (pH 7.4):	32.25
#H bond acceptors:	4	#H bond donors:	2
#Freely Rotating Bonds:	3	Polar Surface Area:	93.45 Å²
Index of Refraction:	1.508	Molar Refractivity:	48.351 cm³
Molar Volume:	162.327 cm³	Polarizability:	19.168 10^-24cm³
Surface Tension:	41.601001739502 dyne/cm	Density:	1.48 g/cm³
Flash Point:	153.225 °C	Enthalpy of Vaporization:	57.226 kJ/mol
Boiling Point:	329.745 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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) =  2.12

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  299.12  (Adapted Stein & Brown method)
    Melting Pt (deg C):  102.86  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  4.36E-005  (Modified Grain method)
    MP  (exp database):  185-188 deg C
    Subcooled liquid VP: 0.00205 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):  418.3
       log Kow used: 2.12 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  7139.6 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   1.01E-010  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  3.294E-008 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  2.12  (KowWin est)
  Log Kaw used:  -8.384  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  10.504
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   0.0532
   Biowin2 (Non-Linear Model)     :   0.0199
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   2.1607  (months      )
   Biowin4 (Primary Survey Model) :   3.3474  (days-weeks  )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :   0.2855
   Biowin6 (MITI Non-Linear Model):   0.0000
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model):  0.6765
 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):  0.273 Pa (0.00205 mm Hg)
  Log Koa (Koawin est  ): 10.504
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  1.1E-005 
       Octanol/air (Koa) model:  0.00783 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  0.000396 
       Mackay model           :  0.000877 
       Octanol/air (Koa) model:  0.385 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant =   3.0617 E-12 cm3/molecule-sec
      Half-Life =     3.494 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =    41.922 Hrs
   Ozone Reaction:
      No Ozone Reaction Estimation
   Fraction sorbed to airborne particulates (phi): 0.000637 (Junge,Mackay)
    Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
      Koc    :  152.9
      Log Koc:  2.184 

 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]:
  Total Kb for pH > 8 at 25 deg C :  3.776E-002  L/mol-sec
  Kb Half-Life at pH 8:     212.462  days   
  Kb Half-Life at pH 7:       5.817  years  

 Bioaccumulation Estimates from Log Kow (BCFWIN v2.17):
   Log BCF from regression-based method = 0.929 (BCF = 8.488)
       log Kow used: 2.12 (estimated)

 Volatilization from Water:
    Henry LC:  1.01E-010 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 8.984E+006  hours   (3.743E+005 days)
    Half-Life from Model Lake : 9.801E+007  hours   (4.084E+006 days)

 Removal In Wastewater Treatment:
    Total removal:               2.37  percent
    Total biodegradation:        0.10  percent
    Total sludge adsorption:     2.27  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       0.000687        83.9         1000       
   Water     20.7            1.44e+003    1000       
   Soil      79.2            2.88e+003    1000       
   Sediment  0.0953          1.3e+004     0          
     Persistence Time: 2.01e+003 hr

Patents	Personal Collections
Publication or Magazine Article	Web-based Article (blog or commentary)
Available Chemicals Databases	Biological Properties
Chemical Reactions	Chemical Safety Data
Drugs or Compounds in Development	Imaging Agents
Information Aggregators	Journal Publishers via MeSH
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

Category	Target	PDB Code	LASSO Score
Kinases	EGFr, epidermal growth factor receptor	1m17	0.07
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.04
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.03
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.02
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.02
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.02
Serine Proteases	FXa, factor Xa	1f0r	0.02
Kinases	TK, thymidine kinase	1kim	0.02
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Kinases	HSP90, human heat shock protein 90	1uy6	0.01
Other Enzymes	ALR2, aldose reductase	1ah3	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.01
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.01
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.01
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.01
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.01
Other Enzymes	AmpC, AmpC beta-lactamase	1xgj	0.00
Other Enzymes	PNP, purine nucleoside phosphorylase	1b8o	0.00
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; agonist	1l2i	0.00
Folate Enzymes	DHFR, dihydrofolate reductase	3dfr	0.00
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.00
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Other Enzymes	HIVPR, HIV protease	1hpx	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Serine Proteases	Thrombin	1ba8	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Serine Proteases	Trypsin	1bju	0.00

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Ethyl 2-amino-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate

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Std. InChI:

Std. InChIKey:

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Ethyl 2-amino-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate

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