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[ CAS No. 27328-68-3 ] {[proInfo.proName]}

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Chemical Structure| 27328-68-3
Chemical Structure| 27328-68-3
Structure of 27328-68-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 27328-68-3 ]

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Product Details of [ 27328-68-3 ]

CAS No. :27328-68-3 MDL No. :MFCD09835467
Formula : C9H7ClN2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OIQMRQZOCUNAIN-UHFFFAOYSA-N
M.W : 210.62 Pubchem ID :12470261
Synonyms :

Calculated chemistry of [ 27328-68-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.11
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 52.65
TPSA : 65.98 ?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) : -6.39 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.85
Log Po/w (XLOGP3) : 1.68
Log Po/w (WLOGP) : 1.84
Log Po/w (MLOGP) : 1.34
Log Po/w (SILICOS-IT) : 2.32
Consensus Log Po/w : 1.61

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.55
Solubility : 0.596 mg/ml ; 0.00283 mol/l
Class : Soluble
Log S (Ali) : -2.68
Solubility : 0.44 mg/ml ; 0.00209 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.31
Solubility : 0.103 mg/ml ; 0.000488 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.77

Safety of [ 27328-68-3 ]

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 [ 27328-68-3 ]

* 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 [ 27328-68-3 ]

[ 27328-68-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 63235-32-5 ]
  • [ 27328-68-3 ]
  • 2
  • [ 64-17-5 ]
  • [ 27328-68-3 ]
  • [ 27512-72-7 ]
YieldReaction ConditionsOperation in experiment
Stage 2 (5-Chloro-1H-indazol-3-yl)acetic acid The amino acid obtained in Stage 1 is dissolved with 3 equivalents of sodium hydroxide pellets in 600 ml of water in a three-necked flask equipped with a thermometer, a mechanical stirrer, a dropping funnel and a reflux condenser surmounted by a bubbler. The mixture is brought to 30-40 C. and 5.7 g of active charcoal are added. Hydrazine monohydrate is slowly added (2.1 eq, i.e. 22.7 g). The mixture is stirred for 15 minutes at 30-40 C. and then for 3 hours at 80-85 C. The reaction mixture is cooled. After filtration, the reaction mixture is acidified with 75 ml of 36% hydrochloric acid. The precipitate formed is filtered off on sintered glass and then dried in a desiccator. Melting point: 193 C.
  • 4
  • [ 6628-86-0 ]
  • [ 27328-68-3 ]
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