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[ CAS No. 81237-69-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 81237-69-6
Chemical Structure| 81237-69-6
Structure of 81237-69-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 81237-69-6 ]

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Product Details of [ 81237-69-6 ]

CAS No. :81237-69-6 MDL No. :MFCD08544279
Formula : C9H10BrN Boiling Point : No data available
Linear Structure Formula :- InChI Key :IZCCDTQAIOPIGY-UHFFFAOYSA-N
M.W : 212.09 Pubchem ID :12823199
Synonyms :

Calculated chemistry of [ 81237-69-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 53.48
TPSA : 12.03 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.16 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.18
Log Po/w (XLOGP3) : 2.02
Log Po/w (WLOGP) : 1.56
Log Po/w (MLOGP) : 2.51
Log Po/w (SILICOS-IT) : 3.12
Consensus Log Po/w : 2.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.83
Solubility : 0.313 mg/ml ; 0.00148 mol/l
Class : Soluble
Log S (Ali) : -1.9
Solubility : 2.67 mg/ml ; 0.0126 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -4.14
Solubility : 0.0154 mg/ml ; 0.0000728 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 81237-69-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 81237-69-6 ]

* 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 [ 81237-69-6 ]

[ 81237-69-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 923591-51-9 ]
  • [ 81237-69-6 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; water; In diethyl ether; 2-Acetyl-5-bromo-l,2,3,4-tetrahydroisoquinoline5-Bromo-l,2,3,4-tetrahydroisoquinoline hydrochloride (2.0 g, 8.0 mmol) was taken up in diethyl ether (20 mL) and washed with NaOH (aq, IN), dried (Na2SO4) and concentrated to give the free amine (1.67 g) that was dissolved in pyridine (15 mL) and cooled to 0 0C. Acetic anhydride (0.82 mL, 8.7 mmol) was added dropwise and the reaction was stirred at RT overnight. Azeotropic evaporation with toluene several times gave the product as a white solid (1.9 g, 94%).1H NMR (SOO MHz, DMSO-d6): delta 7.53 - 7.46 (m, IH), 7.27 - 7.11 (m, 2H), 4.66 and 4.61 rotamers 4:6 (s, 2H), 3.73 - 3.66 (m, 2H), 2.83 and 2.71 rotamers 6:4 (t, J= 6.1 Hz, 2H), 2.09 and 2.07 rotamers 6:4 (s, 3H); APCI-MS m/z: 254/256 1:1 [MH+].
  • 2
  • [ 57772-50-6 ]
  • [ 81237-69-6 ]
  • C17H13BrN2O [ No CAS ]
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