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[ CAS No. 137897-99-5 ] {[proInfo.proName]}

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Chemical Structure| 137897-99-5
Chemical Structure| 137897-99-5
Structure of 137897-99-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 137897-99-5 ]

CAS No. :137897-99-5 MDL No. :MFCD01862261
Formula : C12H6Cl4S2 Boiling Point : -
Linear Structure Formula :- InChI Key :JMQANWHMOHXBEA-UHFFFAOYSA-N
M.W : 356.12 Pubchem ID :2735516
Synonyms :

Calculated chemistry of [ 137897-99-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 3
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 84.64
TPSA : 50.6 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -3.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.61
Log Po/w (XLOGP3) : 6.54
Log Po/w (WLOGP) : 7.1
Log Po/w (MLOGP) : 6.52
Log Po/w (SILICOS-IT) : 6.2
Consensus Log Po/w : 6.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -6.46
Solubility : 0.000122 mg/ml ; 0.000000344 mol/l
Class : Poorly soluble
Log S (Ali) : -7.4
Solubility : 0.0000142 mg/ml ; 0.0000000398 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -7.56
Solubility : 0.0000099 mg/ml ; 0.0000000278 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.68

Safety of [ 137897-99-5 ]

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 [ 137897-99-5 ]

* 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 [ 137897-99-5 ]

[ 137897-99-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3032-81-3 ]
  • [ 137897-99-5 ]
YieldReaction ConditionsOperation in experiment
80% With carbon disulfide; cycl-isopropylidene malonate; triethylamine; copper(l) chloride; In N,N-dimethyl-formamide; at 100℃; for 4h;Inert atmosphere; General procedure: A mixture of Meldrum?s acid (1 mmol) and Et3N (2 mmol) in DMF was stirred for 15 min at r.t. Then, CS2 (1 mmol) was added and stirred for 15 min. Then, the obtained mixture was added to a stirred solution of aryl halide (1 mmol) and CuCl (0.1 mmol) in DMF (2 ml), and heated at 100 C for 4h. When the reaction was completed (TLC), the mixture was extracted with CH2Cl2 (3 3ml) and H2O (3ml). The organic layer was separated and dried (Na2SO4) and the solvent was evaporated in vacuo to give the diaryl disulfide. The product was purified by column chromatography on silica gel (EtOAc / Petroleum ether, 1:4).
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