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[ CAS No. 5965-53-7 ] {[proInfo.proName]}

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Chemical Structure| 5965-53-7
Chemical Structure| 5965-53-7
Structure of 5965-53-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5965-53-7 ]

CAS No. :5965-53-7 MDL No. :MFCD00032382
Formula : C9H14O5 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NGRAIMFUWGFAEM-UHFFFAOYSA-N
M.W : 202.20 Pubchem ID :80070
Synonyms :

Calculated chemistry of [ 5965-53-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 8
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 48.15
TPSA : 69.67 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.03
Log Po/w (XLOGP3) : 0.49
Log Po/w (WLOGP) : 0.46
Log Po/w (MLOGP) : 0.32
Log Po/w (SILICOS-IT) : 1.21
Consensus Log Po/w : 0.9

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.87
Solubility : 27.0 mg/ml ; 0.134 mol/l
Class : Very soluble
Log S (Ali) : -1.52
Solubility : 6.07 mg/ml ; 0.03 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.61
Solubility : 5.01 mg/ml ; 0.0248 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.12

Safety of [ 5965-53-7 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5965-53-7 ]

* 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 [ 5965-53-7 ]

[ 5965-53-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5965-53-7 ]
  • [ 69134-53-8 ]
YieldReaction ConditionsOperation in experiment
33% In tetrahydrofuran; at 0 - 20℃; for 24.0h;Inert atmosphere; To a solution of 2-oxoglutarate ester (0.6 mmol) intetrahydrofuran (THF) (20.0 mL) at 0 C, under argonatmosphere was added NaBH4 (2.0 eq., 1.2 mmol). Themixture was stirred 24 h at room temperature and citricacid was added until the pH reaches 5-6. Then, silicagel (250 mg) was added to the reaction mixture and thesolvent was evaporated under reduced pressure. Theresidue was purified by silica gel column chromatography(EtOAc:hexane 1:1) to afford the respective alpha-hydroxyesters as a colorless oil.Diethyl 2-hydroxyglutarate (4a)Yield 33%; 1H NMR (CDCl3, 200 MHz) d 1.23 (t,J 7.7 Hz, 3H), 1.27 (t, J 7.7 Hz, 3H), 1.84-1.98 (m, 1H),2.06-2.22 (m, 1H), 2.41-2.49 (m, 2H), 3.10 (br s, 1H),4.05-4.27 (m, 5H); 13C NMR (CDCl3, 50 MHz) d 14.1, 29.3,29.7, 60.5, 61.8, 69.5, 173.1, 174.6; IR (film) n / cm-1 3500,2954, 1732, 1440, 1215, 1107; GC (FID) tR (R): 41.3 minand tR (S): 41.8 min; TLC (EtOAc:hexane 1:1) Rf = 0.40.
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