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[ CAS No. 253787-45-0 ] {[proInfo.proName]}

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Chemical Structure| 253787-45-0
Chemical Structure| 253787-45-0
Structure of 253787-45-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 253787-45-0 ]

CAS No. :253787-45-0 MDL No. :MFCD12963565
Formula : C11H8BrNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CSGDGTYOZTXOBR-UHFFFAOYSA-N
M.W : 266.09 Pubchem ID :46835721
Synonyms :

Calculated chemistry of [ 253787-45-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.09
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 60.72
TPSA : 39.19 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.98 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.35
Log Po/w (XLOGP3) : 2.73
Log Po/w (WLOGP) : 2.78
Log Po/w (MLOGP) : 2.32
Log Po/w (SILICOS-IT) : 2.96
Consensus Log Po/w : 2.63

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.57
Solubility : 0.0715 mg/ml ; 0.000269 mol/l
Class : Soluble
Log S (Ali) : -3.21
Solubility : 0.165 mg/ml ; 0.000621 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.63
Solubility : 0.00622 mg/ml ; 0.0000234 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.59

Safety of [ 253787-45-0 ]

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 [ 253787-45-0 ]

* 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 [ 253787-45-0 ]

[ 253787-45-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 2840-29-1 ]
  • [ 56-81-5 ]
  • [ 253787-45-0 ]
YieldReaction ConditionsOperation in experiment
85% A solution of <strong>[2840-29-1]3-amino-4-bromobenzoic acid</strong> (3.6 g, 17 mmol), glycerol (2.4 mL, 33 mmol), and 3-nitrobenzenesulfonic acid sodium salt (11 g, 50 mmol) in 75% H2SO4 (aq.) (40 mL) was stirred at 100 C. for 2 h and 140 C. for 1 h. The reaction mixture was cooled to rt and MeOH (40 mL) was added. The reaction was stirred at 60 C. After 18 h, the mixture was cooled to rt, poured into ice water and made basic with 12 M NH4OH (aq.). EtOAc was added and the solution was filtered. The layers were separated and the aqueous layer was extracted with EtOAc (2*). The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated. The crude product was purified by flash column chromatography (120 g silica gel cartridge; A=Hex, B=EtOAc; 30 min grad.; 0% B to 70% B; flow rate=80 mL/min). The pure fractions were combined, concentrated and dried in vacuo to provide the title compound (3.8 g, 14 mmol, 85% yield) as a white solid. 1H NMR (500 MHz, CHLOROFORM-d) delta 9.48-9.35 (m, 1H), 9.10 (dd, J=3.9, 1.7 Hz, 1H), 8.17-8.05 (m, 2H), 7.60 (dd, J=8.8, 4.1 Hz, 1H), 4.02 (s, 3H). MS (ESI) 265.8, 267.8 (M+H).
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