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[ CAS No. 3102-87-2 ] {[proInfo.proName]}

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Chemical Structure| 3102-87-2
Chemical Structure| 3102-87-2
Structure of 3102-87-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3102-87-2 ]

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Product Details of [ 3102-87-2 ]

CAS No. :3102-87-2 MDL No. :MFCD00007905
Formula : C10H16N2 Boiling Point : -
Linear Structure Formula :(CH3)4C6(NH2)2 InChI Key :WCZNKVPCIFMXEQ-UHFFFAOYSA-N
M.W : 164.25 Pubchem ID :76548
Synonyms :

Calculated chemistry of [ 3102-87-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.4
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 2.0
Molar Refractivity : 55.11
TPSA : 52.04 ?2

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 : Yes
Log Kp (skin permeation) : -5.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.81
Log Po/w (XLOGP3) : 2.02
Log Po/w (WLOGP) : 2.1
Log Po/w (MLOGP) : 2.1
Log Po/w (SILICOS-IT) : 2.26
Consensus Log Po/w : 2.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.5
Solubility : 0.518 mg/ml ; 0.00316 mol/l
Class : Soluble
Log S (Ali) : -2.74
Solubility : 0.299 mg/ml ; 0.00182 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.22
Solubility : 0.0992 mg/ml ; 0.000604 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 3102-87-2 ]

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

Application In Synthesis of [ 3102-87-2 ]

* 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 [ 3102-87-2 ]

[ 3102-87-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2631-77-8 ]
  • [ 3102-87-2 ]
  • C24H20I4N2O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
62% In ethanol; for 3h;Reflux; L1 was synthesized using a modified literatureprocedure.10-13 An ethanolic solution (15 mL) of3,5-diiodine-2-hydroxybenzaldehyde (1.244 g, 2 mmol)was added dropwise to an ethanolic solution (15 mL) of2,3,5,6-tetramethylphenylenediamine (0.164 g, 1 mmol).The reaction mixture was refluxed for 3 h and then stirredovernight at room temperature. Subsequently, the resultingyellow solution was cooled, affording a yellow precipitate,which was filtered off and washed with hexane. Yield:62%; mp > 300 C; elemental analysis for C24H20N2O2I4(anal. calcd. (found)): C, 32.89 (32.70); H, 2.28 (2.45),N: 3.19 (3.30); IR (KBr, ± 4 cm-1) υ / cm-1 3433 (O-H),2916 (C-H, aromatic), 1617 (C=N, imine), 1545 and1432 (C=C, aromatic), 1277 (C-N), 1155 and 1064(C-O, phenol), 645 (C-I); 1H NMR (300 MHz, CDCl3,25 C) δ 8.23 (s, 2H, CH=N), 7.24-7.05 (m, 4H, ArH),2.35 (s, 12H, CH3).
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