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[ CAS No. 1201-74-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1201-74-7
Chemical Structure| 1201-74-7
Structure of 1201-74-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1201-74-7 ]

CAS No. :1201-74-7 MDL No. :MFCD00014321
Formula : C12H13N Boiling Point : No data available
Linear Structure Formula :C10H7CH(NH2)CH3 InChI Key :KHSYYLCXQKCYQX-UHFFFAOYSA-N
M.W : 171.24 Pubchem ID :3857145
Synonyms :

Calculated chemistry of [ 1201-74-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 56.43
TPSA : 26.02 ?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) : -5.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 2.42
Log Po/w (WLOGP) : 2.54
Log Po/w (MLOGP) : 2.85
Log Po/w (SILICOS-IT) : 2.77
Consensus Log Po/w : 2.54

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.93
Solubility : 0.201 mg/ml ; 0.00118 mol/l
Class : Soluble
Log S (Ali) : -2.61
Solubility : 0.421 mg/ml ; 0.00246 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.14
Solubility : 0.0123 mg/ml ; 0.0000718 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.12

Safety of [ 1201-74-7 ]

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 [ 1201-74-7 ]

* 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 [ 1201-74-7 ]

[ 1201-74-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 941-91-3 ]
  • [ 1201-74-7 ]
  • C22H20N2O [ No CAS ]
  • 2
  • [ 1201-74-7 ]
  • [ 161622-05-5 ]
  • [ 1415400-93-9 ]
YieldReaction ConditionsOperation in experiment
95% With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine; In dichloromethane; acetonitrile; at 20℃; General procedure: A mixture of 1 mmol (1 equiv.) of carboxylic acids, 1.4 mmol (1.4 equiv.) of amine, 552 mg (1.8 equiv.) of PyBOP and 2 mL of triethylamine was stirred overnight at room temperature in 40 ml of a 1:1 mixture of CH2Cl2 and CH3CN. After solvent evaporation, the crude product was purified by column chromatography on silica (CHCl3:CH3CH2OH = 9:1) resulting in yellow thick oil that slowly crystallized.
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