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[ CAS No. 188815-32-9 ] {[proInfo.proName]}

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Chemical Structure| 188815-32-9
Chemical Structure| 188815-32-9
Structure of 188815-32-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 188815-32-9 ]

CAS No. :188815-32-9 MDL No. :MFCD00191851
Formula : C7H4BrIO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MKJBJYCBKXPQSY-UHFFFAOYSA-N
M.W : 326.91 Pubchem ID :5182520
Synonyms :

Calculated chemistry of [ 188815-32-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 53.82
TPSA : 37.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.88
Log Po/w (XLOGP3) : 2.79
Log Po/w (WLOGP) : 2.75
Log Po/w (MLOGP) : 3.24
Log Po/w (SILICOS-IT) : 2.86
Consensus Log Po/w : 2.7

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.96
Solubility : 0.0357 mg/ml ; 0.000109 mol/l
Class : Soluble
Log S (Ali) : -3.23
Solubility : 0.193 mg/ml ; 0.000589 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.55
Solubility : 0.0926 mg/ml ; 0.000283 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.82

Safety of [ 188815-32-9 ]

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

Application In Synthesis of [ 188815-32-9 ]

* 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 [ 188815-32-9 ]

[ 188815-32-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56622-54-9 ]
  • [ 188815-32-9 ]
  • [ 1217484-59-7 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; To a stirred mixture of 3-bromo-5-iodo-benzoic acid (1.4 g, 4.4 mmol), N-(3- dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (1.7 g, 8.8 mmol), 1 -hydroxybenzotriazole hydrate (0.20 g, 1.3 mmol), and CH2Cl2 (50 mL) were added <strong>[56622-54-9](6-methylpyridin-3-yl)methanamine</strong> (0.65 g, 5.3 mmol) and N,N-diisopropylethylamine (1.5 mL, 8.8 mmol). The reaction mixture was stirred at room temperature overnight and then concentrated in vacuo. The precipitated solid was washed with water and ethyl ether and dried to afford the product as a white solid. LC-MS: 432.7 [M+l]+.
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