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[ CAS No. 22921-68-2 ] {[proInfo.proName]}

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Chemical Structure| 22921-68-2
Chemical Structure| 22921-68-2
Structure of 22921-68-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 22921-68-2 ]

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Product Details of [ 22921-68-2 ]

CAS No. :22921-68-2 MDL No. :MFCD00020214
Formula : C8H7BrO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ODHJOROUCITYNF-UHFFFAOYSA-N
M.W : 231.04 Pubchem ID :89906
Synonyms :

Calculated chemistry of [ 22921-68-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.59
TPSA : 46.53 ?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) : -6.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.72
Log Po/w (XLOGP3) : 2.14
Log Po/w (WLOGP) : 2.16
Log Po/w (MLOGP) : 2.06
Log Po/w (SILICOS-IT) : 1.89
Consensus Log Po/w : 1.99

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.86
Solubility : 0.32 mg/ml ; 0.00138 mol/l
Class : Soluble
Log S (Ali) : -2.75
Solubility : 0.412 mg/ml ; 0.00178 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.76
Solubility : 0.403 mg/ml ; 0.00175 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 22921-68-2 ]

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 [ 22921-68-2 ]

* 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 [ 22921-68-2 ]
  • Downstream synthetic route of [ 22921-68-2 ]

[ 22921-68-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 6313-33-3 ]
  • [ 22921-68-2 ]
  • [ 19181-64-7 ]
YieldReaction ConditionsOperation in experiment
55% With 8-quinolinol; sodium hydroxide; copper dichloride In water at 20℃; for 0.333333 h; Sealed tube; Microwave irradiation General procedure: In a 10 mL glass tube 2-iodobenzoic acid (1.0 mmol), acetamidine hydrochloride (1.2 mmol), CuCl2 (0.1 mmol), L2 (0.1 mmol), and NaOH (4.0 equiv.) and 3.0 mL water were placed. The vessel was then sealed with a septum and placed into the microwave cavity. Initial microwave irradiation of 120 W by using a CEM Discover microwave synthesizer was used at the room temperature for 20 min. The reaction mixture was stirred continuously during the reaction. After completion of the reaction, the solvent was removed in vacuo. The residue was purified by silica gel column chromatography to afford the corresponding product. All the products were confirmed by NMR and MS spectroscopic analysis.
Reference: [1] Synthetic Communications, 2018, vol. 48, # 24, p. 3089 - 3098
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