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[ CAS No. 21109-25-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 21109-25-1
Chemical Structure| 21109-25-1
Structure of 21109-25-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 21109-25-1 ]

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Product Details of [ 21109-25-1 ]

CAS No. :21109-25-1 MDL No. :MFCD03422512
Formula : C9H10N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RNAODKZCUVVPEN-UHFFFAOYSA-N
M.W : 146.19 Pubchem ID :582331
Synonyms :

Calculated chemistry of [ 21109-25-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.11
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 2.0
Molar Refractivity : 45.97
TPSA : 41.81 ?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 : No
Log Kp (skin permeation) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.4
Log Po/w (XLOGP3) : 0.94
Log Po/w (WLOGP) : 1.47
Log Po/w (MLOGP) : 0.96
Log Po/w (SILICOS-IT) : 2.14
Consensus Log Po/w : 1.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.88
Solubility : 1.94 mg/ml ; 0.0132 mol/l
Class : Very soluble
Log S (Ali) : -1.4
Solubility : 5.76 mg/ml ; 0.0394 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.31
Solubility : 0.0721 mg/ml ; 0.000493 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.19

Safety of [ 21109-25-1 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 21109-25-1 ]

* 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 [ 21109-25-1 ]

[ 21109-25-1 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 1670-84-4 ]
  • [ 21109-25-1 ]
YieldReaction ConditionsOperation in experiment
With dimethylsulfide borane complex; In tetrahydrofuran; at 0 - 60℃; for 3h; To a solution of the crude amide obtained in the above step (1) inTHF (30 ml), BMS (1.18 ml, 12.42 mmol) was slowly added at 0 °C. Theresulting reaction mixture was heated to 60 °C for 3hrs, quenched with 5percent HCIat 0 °C, extracted with EA, and washed with 5percent HCI. The aqueous layerswere combined and basified with 1N NaOH, and again extracted with EA.The organic layers were combined and concentrated to obtain the titlecompound (0.28 g) as yellow oil.TLC System 1 : MC/MeOH =90:10 v/v Rf=0.151H-NMR (300MHz, CDCI3) 8 ppm: 3.98(s, 2H), 7.08(m, 3H),7.26(m, 1H), 7.58(d, 1H), 9.10(brs,
  • 2
  • [ 21109-25-1 ]
  • [ 22980-09-2 ]
  • 2-(1<i>H</i>-indol-3-yl)-<i>N</i>-(1<i>H</i>-indol-2-ylmethyl)-2-oxo-acetamide [ No CAS ]
  • 3
  • [ 75-15-0 ]
  • [ 21109-25-1 ]
  • [ 100-39-0 ]
  • (1<i>H</i>-indol-2-ylmethyl)-dithiocarbamic acid benzyl ester [ No CAS ]
  • 4
  • [ 21109-25-1 ]
  • [ 6953-35-1 ]
  • <i>N</i>-(1<i>H</i>-indol-2-ylmethyl)-2-(5-nitro-1<i>H</i>-indol-3-yl)-2-oxo-acetamide [ No CAS ]
  • 5
  • [ 21109-25-1 ]
  • [ 103-72-0 ]
  • [ 917986-04-0 ]
  • 6
  • [ 21109-25-1 ]
  • [ 556-61-6 ]
  • [ 80412-16-4 ]
  • 8
  • [ 881853-73-2 ]
  • [ 21109-25-1 ]
  • 9
  • [ 21109-25-1 ]
  • [ 874-60-2 ]
  • [ 943188-11-2 ]
  • 10
  • [ 21109-25-1 ]
  • [ 393-52-2 ]
  • [ 895944-53-3 ]
  • 11
  • [ 21109-25-1 ]
  • [ 2168-78-7 ]
  • [ 943188-12-3 ]
  • 12
  • [ 21109-25-1 ]
  • [ 5990-17-0 ]
  • [ 943188-13-4 ]
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