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[ CAS No. 205448-65-3 ] {[proInfo.proName]}

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Chemical Structure| 205448-65-3
Chemical Structure| 205448-65-3
Structure of 205448-65-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 205448-65-3 ]

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Product Details of [ 205448-65-3 ]

CAS No. :205448-65-3 MDL No. :MFCD13192255
Formula : C12H11NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :TYKSVPGCVLNVIO-UHFFFAOYSA-N
M.W : 233.22 Pubchem ID :22646623
Synonyms :

Calculated chemistry of [ 205448-65-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.17
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.34
TPSA : 68.39 ?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) : -6.74 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.04
Log Po/w (XLOGP3) : 1.38
Log Po/w (WLOGP) : 1.32
Log Po/w (MLOGP) : 0.42
Log Po/w (SILICOS-IT) : 2.45
Consensus Log Po/w : 1.52

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.39
Solubility : 0.944 mg/ml ; 0.00405 mol/l
Class : Soluble
Log S (Ali) : -2.42
Solubility : 0.888 mg/ml ; 0.00381 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.82
Solubility : 0.0354 mg/ml ; 0.000152 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.84

Safety of [ 205448-65-3 ]

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 [ 205448-65-3 ]

* 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 [ 205448-65-3 ]

[ 205448-65-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 205448-65-3 ]
  • [ 417721-36-9 ]
YieldReaction ConditionsOperation in experiment
87% With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 9h; 5 g (0.022 mmol) of compound 5 was weighed into a single-necked flask, and 30 mL of dichloromethane and 3 D of DMF were added thereto, and oxalyl chloride was added dropwise at room temperature for 9 hours. After cooling to room temperature, dichloromethane was evaporated under reduced pressure, and ethyl acetate was added thereto, followed by rotary distillation, and the mixture was stirred twice to chloroformyl chloride. The mixture was evaporated to 20 mL of methanol and 50 mL of aqueous ammonia. After cooling to room temperature, suction filtration, the filter cake was washed with water and dried to give a brown-yellow solid (6) 3.89 g, yield 87%.
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