General Information

Mainterm3,3,3-trifluoropropene
CAS Reg.No.(or other ID)677-21-4
Regnum

From www.fda.gov

Computed Descriptors

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2D Structure
CID12672
IUPAC Name3,3,3-trifluoroprop-1-ene
InChIInChI=1S/C3H3F3/c1-2-3(4,5)6/h2H,1H2
InChI KeyFDMFUZHCIRHGRG-UHFFFAOYSA-N
Canonical SMILESC=CC(F)(F)F
Molecular FormulaC3H3F3
Wikipediatrifluoropropene

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight96.052
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Complexity51.5
CACTVS Substructure Key Fingerprint A A A D c Q B A A Y A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A G Q A A A A A A C A C A A B A A A A A A A A C A A C B C A A A A A A A A A A A I A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = =
Topological Polar Surface Area0.0
Monoisotopic Mass96.019
Exact Mass96.019
XLogP3None
XLogP3-AA2.0
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count6
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9891
Human Intestinal AbsorptionHIA+0.9946
Caco-2 PermeabilityCaco2+0.6559
P-glycoprotein SubstrateNon-substrate0.8701
P-glycoprotein InhibitorNon-inhibitor0.9092
Non-inhibitor0.9094
Renal Organic Cation TransporterNon-inhibitor0.9207
Distribution
Subcellular localizationMitochondria0.5365
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8699
CYP450 2D6 SubstrateNon-substrate0.6027
CYP450 3A4 SubstrateNon-substrate0.7362
CYP450 1A2 InhibitorNon-inhibitor0.6782
CYP450 2C9 InhibitorNon-inhibitor0.8235
CYP450 2D6 InhibitorNon-inhibitor0.9528
CYP450 2C19 InhibitorNon-inhibitor0.7496
CYP450 3A4 InhibitorNon-inhibitor0.8903
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8780
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9734
Non-inhibitor0.9326
AMES ToxicityNon AMES toxic0.7792
CarcinogensCarcinogens 0.6820
Fish ToxicityHigh FHMT0.9640
Tetrahymena Pyriformis ToxicityHigh TPT0.9929
Honey Bee ToxicityHigh HBT0.8923
BiodegradationNot ready biodegradable0.9857
Acute Oral ToxicityIII0.6436
Carcinogenicity (Three-class)Non-required0.5647

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.2002LogS
Caco-2 Permeability1.5429LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.0511LD50, mol/kg
Fish Toxicity0.2959pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.7761pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganohalogen compounds
ClassOrganofluorides
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentOrganofluorides
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsHydrofluorocarbon - Hydrocarbon derivative - Organofluoride - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as organofluorides. These are compounds containing a chemical bond between a carbon atom and a fluorine atom.

From ClassyFire