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[ CAS No. 41841-16-1 ] {[proInfo.proName]}

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Chemical Structure| 41841-16-1
Chemical Structure| 41841-16-1
Structure of 41841-16-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 41841-16-1 ]

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Product Details of [ 41841-16-1 ]

CAS No. :41841-16-1 MDL No. :MFCD00126844
Formula : C9H9BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QHJOWSXZDCTNQX-UHFFFAOYSA-N
M.W : 229.07 Pubchem ID :316783
Synonyms :

Calculated chemistry of [ 41841-16-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 50.01
TPSA : 26.3 ?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) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.44
Log Po/w (XLOGP3) : 2.52
Log Po/w (WLOGP) : 2.16
Log Po/w (MLOGP) : 2.7
Log Po/w (SILICOS-IT) : 2.71
Consensus Log Po/w : 2.51

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.02
Solubility : 0.219 mg/ml ; 0.000955 mol/l
Class : Soluble
Log S (Ali) : -2.72
Solubility : 0.438 mg/ml ; 0.00191 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.74
Solubility : 0.0419 mg/ml ; 0.000183 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 41841-16-1 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H227-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 41841-16-1 ]

* 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 [ 41841-16-1 ]

[ 41841-16-1 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 721960-43-6 ]
  • [ 41841-16-1 ]
  • [ 871476-59-4 ]
YieldReaction ConditionsOperation in experiment
48% g) Compound 1.8; To a solution of methyl (4-bromophenyl) acetate (obtained from the corresponding acid (267.5 mg, 1.2 mmol) upon treatment with excess diazomethane) in 1,4-dioxane (5 mL) were added intermediate 1.7 (315 mg, 1.20 mmol) and K3P04 (792 mg, 3.73 mmol). After degassing the reaction mixture for 45 min, PdCl2 (dppf) mg, 0.19 mmol) and dppf (136 mg, 0.06 mmol) were added and the mixture was heated at 100C for 3 h. After cooling to room temperature the reaction mixture was diluted with EtOAc, washed successively with water and brine, dried (MgS04), filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using hexane/EtOAc (80/20) to give compound 1.8 (164 mg, 48% yield)
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Technical Information

Historical Records

Pharmaceutical Intermediates of
[ 41841-16-1 ]

Macitentan Intermediates

Chemical Structure| 706811-25-8

[ 706811-25-8 ]

5-(4-Bromophenyl)-6-hydroxypyrimidin-4(1H)-one

Chemical Structure| 146533-41-7

[ 146533-41-7 ]

5-(4-Bromophenyl)-4,6-dichloropyrimidine

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[ 6313-33-3 ]

Formimidamide hydrochloride

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[ 1878-68-8 ]

4-Bromophenylacetic acid

Chemical Structure| 147962-41-2

[ 147962-41-2 ]

N-Propylsulfamide

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