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[ CAS No. 89364-06-7 ]

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3d Animation Molecule Structure of 89364-06-7
Chemical Structure| 89364-06-7
Chemical Structure| 89364-06-7
Structure of 89364-06-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 89364-06-7 ]

CAS No. :89364-06-7 MDL No. :MFCD12913282
Formula : C5H3ClN4 Boiling Point : -
Linear Structure Formula :- InChI Key :MSGJNOUXBKOZPT-UHFFFAOYSA-N
M.W :154.56 g/mol Pubchem ID :21766613
Synonyms :

Calculated chemistry of [ 89364-06-7 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 35.79
TPSA : 43.08 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.26
Log Po/w (XLOGP3) : 1.06
Log Po/w (WLOGP) : 0.78
Log Po/w (MLOGP) : 0.39
Log Po/w (SILICOS-IT) : 0.74
Consensus Log Po/w : 0.84

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.13
Solubility : 1.14 mg/ml ; 0.00738 mol/l
Class : Soluble
Log S (Ali) : -1.56
Solubility : 4.3 mg/ml ; 0.0278 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.94
Solubility : 1.77 mg/ml ; 0.0115 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.78

Safety of [ 89364-06-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 89364-06-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 89364-06-7 ]

[ 89364-06-7 ] Synthesis Path-Downstream   1~1

YieldReaction ConditionsOperation in experiment
5,7-Dichlor-s-triazolo<2,3-a>pyrimidin, Na2CO3, H2 (1 Mol), Pd-Kohle, abs.A.;
s-Triazolo<1.5-a>pyrimidin 10,POCl3;
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