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[ CAS No. 40928-13-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 40928-13-0
Chemical Structure| 40928-13-0
Structure of 40928-13-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 40928-13-0 ]

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Product Details of [ 40928-13-0 ]

CAS No. :40928-13-0 MDL No. :MFCD00090431
Formula : C8H4ClNO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QRUPDIJQZCABTC-UHFFFAOYSA-N
M.W : 197.58 Pubchem ID :329105
Synonyms :

Calculated chemistry of [ 40928-13-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.11
TPSA : 63.07 ?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) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.23
Log Po/w (XLOGP3) : 1.65
Log Po/w (WLOGP) : 1.13
Log Po/w (MLOGP) : 1.59
Log Po/w (SILICOS-IT) : 2.71
Consensus Log Po/w : 1.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.67
Solubility : 0.419 mg/ml ; 0.00212 mol/l
Class : Soluble
Log S (Ali) : -2.59
Solubility : 0.51 mg/ml ; 0.00258 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.77
Solubility : 0.0339 mg/ml ; 0.000171 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.57

Safety of [ 40928-13-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 40928-13-0 ]

* 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 [ 40928-13-0 ]

[ 40928-13-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 40928-13-0 ]
  • [ 112734-22-2 ]
  • 2-amino-N-(4-bromo-2-fluorobenzyl)-4-chlorobenzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; PREPARATION 11 A mixture of 7-chloro-2H-3,1-benzoxazine-2,4(1H)dione (18.4 g) and <strong>[112734-22-2]4-bromo-2-fluorobenzylamine</strong> (26 g) in tetrahydrofuran (200 ml) was refluxed for 15 minutes. After cooling, tetrahydrofuran was evaporated to give a residue. Recrystallization from isopropyl ether gave 2-amino-N-(4-bromo-2-fluorobenzyl)-4-chlorobenzamide (26.6 g). mp: 119.5 C. IR (Nujol): 3460, 3350, 3260, 1625, 1605 cm-1. NMR (DMSO-d6, delta): 4.4 (2H, d, J=5.6 Hz), 6.5-6.8 (4H, m), 7.3-7.6 (4H, m), 8.8 (1H, t, J=5.6 Hz).
  • 2
  • [ 40928-13-0 ]
  • [ 5900-59-4 ]
YieldReaction ConditionsOperation in experiment
With ammonium carbonate; In 1,4-dioxane; at 60℃; General procedure: Compound 13 was prepared according to the procedurepreviously reported.37 A suspension of isatoic anhydride 12 (40mmol), ammonium carbonate (160 mmol), and 1,4-dioxane(150 mL) was heated at 60 C. After being stirred for 5-8 h,the reaction mixture was cooled to room temperature andevaporated under reduced pressure, and then water (200 mL)was added to the residue, which was extracted three times withEtOAc (300 mL). The organic layer was washed with brine(100 mL), dried over anhydrous Na2SO4, filtered, andconcentrated to afford compound 13 in yields of 80-85%.
With ammonium carbonate; In 1,4-dioxane; at 60℃; for 8h; General procedure: A suspension of isatoic anhydride (35 mmol), ammonium carbonate (140 mmol), and 1,4-dioxane (150 mL) was heated at 60 C. After stirring for 8 h, the reaction mixture was cooled to room temperature and evaporated underreduced pressure, and then water (200 mL) was added to the residue, which was extracted with DCM (80 mL × 3). The organic layerwas dried over anhydrous Na2SO4, and concentrated to give compound 3 in yield of 84%.
With ammonium carbonate; In 1,4-dioxane; at 60℃; for 8h; General procedure: A suspension of substituted isatoic anhydride (35 mmol), ammonium carbonate (140 mmol), and 1,4-dioxane (150 mL) was heated at 60 C. After stirring for 8 h, the reaction mixture was cooled to room temperature and evaporated under reduced pressure, and then water (200 mL) was added to the residue, which was extracted with CH2Cl2 (380 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated to give compounds 9 in yields of 63-94%.
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