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[ CAS No. 898543-06-1 ] {[proInfo.proName]}

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Chemical Structure| 898543-06-1
Chemical Structure| 898543-06-1
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Product Details of [ 898543-06-1 ]

CAS No. :898543-06-1 MDL No. :MFCD20133901
Formula : C14H18ClN3O4 Boiling Point : -
Linear Structure Formula :- InChI Key :ITMQDYQHNKXERQ-YDALLXLXSA-N
M.W : 327.76 Pubchem ID :16037077
Synonyms :

Calculated chemistry of [ 898543-06-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 22
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.43
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 88.36
TPSA : 85.1 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -8.02 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.4
Log Po/w (WLOGP) : 0.37
Log Po/w (MLOGP) : 0.35
Log Po/w (SILICOS-IT) : 0.18
Consensus Log Po/w : 0.26

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.13
Solubility : 2.44 mg/ml ; 0.00745 mol/l
Class : Soluble
Log S (Ali) : -1.75
Solubility : 5.78 mg/ml ; 0.0176 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.08
Solubility : 2.75 mg/ml ; 0.00839 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.05

Safety of [ 898543-06-1 ]

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

Application In Synthesis of [ 898543-06-1 ]

* 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 [ 898543-06-1 ]

[ 898543-06-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35475-03-7 ]
  • [ 898543-06-1 ]
  • [ 366789-02-8 ]
YieldReaction ConditionsOperation in experiment
at 120℃; for 48h;Inert atmosphere; Heating;Product distribution / selectivity; 20 gms of 4-{4-[(5S)-5-(Aminomethyl)-2-oxo-l,3-oxazolidin-3-yl]phenyl}-morpholin- 3-one, and 12.13 gms of methyl-5-chlorothiophene-2-carboxylic acid were charged into a clean and dry 500ml. 4 neck R.B. Flask. The reaction mixture was heated to about 120C for about 48 hours under nitrogen. After completion of the reaction, the reaction mass was cooled to about 30C, 180ml of acetic acid was added. The resultant reaction suspension was heated to about 110C, 2.5 gms of charcoal carbon was added. The suspension was filtered and the filtrate was cooled to about 20C for about 15 mins. The solid separated was filtered and the solid was washed with water afford the title compound in pure form.Yield : 26gms.; Purity by HPLC: 99.96%.
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