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[ CAS No. 89-54-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 89-54-3
Chemical Structure| 89-54-3
Structure of 89-54-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 89-54-3 ]

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Product Details of [ 89-54-3 ]

CAS No. :89-54-3 MDL No. :MFCD00007845
Formula : C7H6ClNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :GVCFFVPEOLCYNN-UHFFFAOYSA-N
M.W : 171.58 Pubchem ID :37879
Synonyms :

Calculated chemistry of [ 89-54-3 ]      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 : 2.0
Molar Refractivity : 42.82
TPSA : 63.32 ?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) : -6.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.91
Log Po/w (XLOGP3) : 1.33
Log Po/w (WLOGP) : 1.63
Log Po/w (MLOGP) : 0.48
Log Po/w (SILICOS-IT) : 1.14
Consensus Log Po/w : 1.1

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.08
Solubility : 1.43 mg/ml ; 0.00833 mol/l
Class : Soluble
Log S (Ali) : -2.26
Solubility : 0.941 mg/ml ; 0.00548 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.02
Solubility : 1.63 mg/ml ; 0.00948 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.18

Safety of [ 89-54-3 ]

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

Application In Synthesis of [ 89-54-3 ]

* 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 [ 89-54-3 ]

[ 89-54-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 207981-46-2 ]
  • [ 89-54-3 ]
  • [ 1001340-15-3 ]
YieldReaction ConditionsOperation in experiment
60% In tetrahydrofuran; for 16h; EXAMPLE 26. Synthesis of 2-ChJoro-5-f2-Fluoro-5-TrifluoromethyI-Benzoylamino)-Benzoic Acid (Intermediate 18)18[0162] 5-Amino-2-chIoro-benzoic acid (0.4 g, 2.32 mmol) was diluted with THF (12 mL), treated with 2-fluoro-5-trifluoromethyl-benzoyl chloride (0.388 g, 2.56 mmol) and stirred for 16h. Solvents were then removed and resulting solids were triturated with DCM. After filtration, the title compound was obtained as a white solid (0.5 g, 60%).
  • 2
  • [ 89-54-3 ]
  • [ 3537-14-2 ]
  • 4-chloro-3-[6-nitro-1H-imidazo[4,5-b]pyridin-2-yl]aniline [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% With polyphosphoric acid; at 130℃; for 48h; Into a 1-L round-bottom flask, was placed <strong>[3537-14-2]5-nitropyridine-2,3-diamine</strong> (30 g, 194.65 mmol, 1.00 equiv), 5-amino-2-chlorobenzoic acid (33.4 g, 194.66 mmol, 1.00 equiv), PPA (400 mL). The resulting solution was stirred for 2 days at 130 C. The reaction mixture was cooled with a water/ice bath. The resulting solution was diluted with 400 mL of ice water. The pH value of the solution was adjusted to 7 with sodium hydroxide (5%). The solids were collected by filtration and washed with 3*50 mL water. The solid was dried in an oven under reduced pressure. This resulted in 40 g (71%) of 4-chloro-3-[6-nitro-1H-imidazo[4,5-b]pyridin-2-yl]aniline (I-6) as a yellow solid.
  • 3
  • [ 62171-59-9 ]
  • [ 89-54-3 ]
  • 9,9-dimethyl-9,10-dihydrophenanthren-2-amine [ No CAS ]
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