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[ CAS No. 66607-27-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 66607-27-0
Chemical Structure| 66607-27-0
Structure of 66607-27-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 66607-27-0 ]

CAS No. :66607-27-0 MDL No. :MFCD04972469
Formula : C7H5IN2 Boiling Point : -
Linear Structure Formula :- InChI Key :UDKYMMQGPNFWDA-UHFFFAOYSA-N
M.W : 244.03 Pubchem ID :10911744
Synonyms :

Calculated chemistry of [ 66607-27-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.81
TPSA : 28.68 ?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) : -6.2 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.24
Log Po/w (XLOGP3) : 2.24
Log Po/w (WLOGP) : 2.17
Log Po/w (MLOGP) : 2.31
Log Po/w (SILICOS-IT) : 3.04
Consensus Log Po/w : 2.2

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.43
Solubility : 0.0906 mg/ml ; 0.000371 mol/l
Class : Soluble
Log S (Ali) : -2.48
Solubility : 0.812 mg/ml ; 0.00333 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.87
Solubility : 0.0331 mg/ml ; 0.000136 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.07

Safety of [ 66607-27-0 ]

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 [ 66607-27-0 ]

* 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 [ 66607-27-0 ]

[ 66607-27-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 850568-54-6 ]
  • [ 66607-27-0 ]
  • 4-(3-iodoindazol-1-yl)benzoic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
22.1% With copper diacetate; triethylamine; In dichloromethane; at 20℃; for 16h;Inert atmosphere; 3-Iodo-1H-indazole (5.00 g; 20.5 mmol; 1.00 eq.), triethylamine (5.68 mL; 41.0 mmol; 2.00 eq.), <strong>[850568-54-6]4-(tert-butoxycarbonyl)phenylboronic acid</strong> (9.38 g; 41.0 mmol; 2.00 eq.). and copper acetate (5.58 g; 30.7 mmol; 1.50 eq.) in dichloromethane (80.0 mL), were stirred at room temperature in a round bottom flask for 16 hours. The reaction mixture was cooled to 0 °C. 200 mL mixture of NH4OH / NH4Cl (aq) sat. (1/1) and 50 mL of dichloromethane were added. The aqueous layer was extracted with another 50 mL of dichloromethane. The combined organic phases were washed three times with 50 mL of a saturated solution of NH4OH, and once with 50 mL of water. The organic layer was dried over MgSO4, filtered and concentrated under vacuum. The residue obtained was purified on silica gel chromatography using heptane/dichloromethane (7/3) as eluent. 4-(3-Iodoindazol-1-yl)benzoic acid was isolated as a pale yellow oil. (1.90 g; 22.1percent).
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