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[ CAS No. 2198-66-5 ] {[proInfo.proName]}

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Chemical Structure| 2198-66-5
Chemical Structure| 2198-66-5
Structure of 2198-66-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2198-66-5 ]

CAS No. :2198-66-5 MDL No. :MFCD02682891
Formula : C10H13BrO Boiling Point : -
Linear Structure Formula :C6H3(C(CH3)3)(Br)OH InChI Key :FFRLMQPMGIMHHQ-UHFFFAOYSA-N
M.W : 229.11 Pubchem ID :75147
Synonyms :

Calculated chemistry of [ 2198-66-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.4
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 55.44
TPSA : 20.23 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.63
Log Po/w (XLOGP3) : 3.93
Log Po/w (WLOGP) : 3.45
Log Po/w (MLOGP) : 3.46
Log Po/w (SILICOS-IT) : 3.17
Consensus Log Po/w : 3.33

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.04
Solubility : 0.0209 mg/ml ; 0.0000911 mol/l
Class : Moderately soluble
Log S (Ali) : -4.05
Solubility : 0.0202 mg/ml ; 0.0000883 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -3.89
Solubility : 0.0294 mg/ml ; 0.000128 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.41

Safety of [ 2198-66-5 ]

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 [ 2198-66-5 ]

* 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.

  • Upstream synthesis route of [ 2198-66-5 ]
  • Downstream synthetic route of [ 2198-66-5 ]

[ 2198-66-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 98-54-4 ]
  • [ 98-22-6 ]
  • [ 2198-66-5 ]
YieldReaction ConditionsOperation in experiment
90%
Stage #1: With toluene-4-sulfonic acid In methanol for 0.166667 h;
Stage #2: With N-Bromosuccinimide In methanol for 0.416667 h;
General procedure: A solution of the starting material (~10 mmol) and pTsOH (10 mol percent) in MeOH (1.0 mL per mmol starting material) was stirred for 10 min, then a solution of NBS (100 mol percent; recrystallized from H2O) in MeOH (0.1 M) was added dropwise over 20 min from a foiled reaction flask. The reaction mixture was stirred for a further 5 min and then concentrated in vacuo. The resultant residue was purified using column chromatography (CH2Cl2, or 1percent MeOH in CH2Cl2). 3.3. Characterization of Products2-Bromo-4-methylphenol (10) [23]: 10.1 mmol; 1.73 g (92percent);
Reference: [1] Molecules, 2016, vol. 21, # 1,
[2] Tetrahedron, 2009, vol. 65, # 22, p. 4429 - 4439
[3] Canadian Journal of Chemistry, 2018, vol. 96, # 12, p. 1087 - 1091
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