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[ CAS No. 38240-21-0 ] {[proInfo.proName]}

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Chemical Structure| 38240-21-0
Chemical Structure| 38240-21-0
Structure of 38240-21-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 38240-21-0 ]

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Product Details of [ 38240-21-0 ]

CAS No. :38240-21-0 MDL No. :MFCD09757485
Formula : C5H6N2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :ADMMJKIQWOJMSK-UHFFFAOYSA-N
M.W : 126.18 Pubchem ID :5463181
Synonyms :

Calculated chemistry of [ 38240-21-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 2.0
Molar Refractivity : 36.03
TPSA : 73.9 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.84 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.17
Log Po/w (XLOGP3) : 0.33
Log Po/w (WLOGP) : 1.33
Log Po/w (MLOGP) : -0.34
Log Po/w (SILICOS-IT) : 2.33
Consensus Log Po/w : 0.97

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.39
Solubility : 5.2 mg/ml ; 0.0412 mol/l
Class : Very soluble
Log S (Ali) : -1.45
Solubility : 4.52 mg/ml ; 0.0358 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.73
Solubility : 2.33 mg/ml ; 0.0185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.81

Safety of [ 38240-21-0 ]

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

Application In Synthesis of [ 38240-21-0 ]

* 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 [ 38240-21-0 ]

[ 38240-21-0 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 38240-21-0 ]
  • [ 135-67-1 ]
  • [ 23351-91-9 ]
  • C30H17N5OS2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
21% Except that 3-aminopyridine-2-thiol was used instead of 2-amino-4-hydroxypyridine, and 5-bromoisophthalate replaced by 2,2'-dibromo-4,4'-dicarboxy biphenyl, other synthesis process with Example 22. Purified by silica gel column chromatography to give a solid Compound 12 (9.0g, 21percent yield).
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