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[ CAS No. 13211-32-0 ] {[proInfo.proName]}

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Chemical Structure| 13211-32-0
Chemical Structure| 13211-32-0
Structure of 13211-32-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13211-32-0 ]

CAS No. :13211-32-0 MDL No. :MFCD03452738
Formula : C6H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :HQLILHPGWSURBT-UHFFFAOYSA-N
M.W : 132.16 Pubchem ID :2760998
Synonyms :

Calculated chemistry of [ 13211-32-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 33.85
TPSA : 46.53 ?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) : -6.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.42
Log Po/w (XLOGP3) : 0.66
Log Po/w (WLOGP) : 0.89
Log Po/w (MLOGP) : 0.39
Log Po/w (SILICOS-IT) : 0.25
Consensus Log Po/w : 0.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.88
Solubility : 17.5 mg/ml ; 0.133 mol/l
Class : Very soluble
Log S (Ali) : -1.21
Solubility : 8.09 mg/ml ; 0.0612 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.57
Solubility : 35.2 mg/ml ; 0.267 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.44

Safety of [ 13211-32-0 ]

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

Application In Synthesis of [ 13211-32-0 ]

* 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 [ 13211-32-0 ]

[ 13211-32-0 ] Synthesis Path-Downstream   1~15

  • 1
  • [ 100-02-7 ]
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  • [ 6377-28-2 ]
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  • [ 46744-54-1 ]
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  • 3
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  • [ 16071-39-9 ]
  • 5
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  • [ 100-14-1 ]
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  • 6
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  • [ 107-14-2 ]
  • [ 6403-40-3 ]
  • 7
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  • [ 79-11-8 ]
  • [ 6377-28-2 ]
  • 8
  • [ 79-11-8 ]
  • [ 865-48-5 ]
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  • 9
  • [ 4291-69-4 ]
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  • [ 78890-63-8 ]
  • [ 78890-62-7 ]
  • 10
  • [ 4798-46-3 ]
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  • [ 125641-74-9 ]
  • 11
  • [ 107-71-1 ]
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  • 12
  • [ 1634-04-4 ]
  • [ 124-38-9 ]
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  • 13
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  • [ 5042-55-7 ]
  • [ 116193-69-2 ]
  • 15
  • [ 116193-68-1 ]
  • [ 13211-32-0 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; EXAMPLE 2 2-tert-Butoxyacetic acid To 100 ml of a 50:50 (v/v) methanol/water solution containing 14.35 g of potassium carbonate, was added n-butyl 2-tert-butoxyacetate (6.50 g, 0.0346 mol). The mixture was heated at reflux for 17 hours and the volatiles removed on a flash evaporator. The remaining solution was cooled to approximately 0° C. and acidified to pH 3-4 with cold 50percent aqueous hydrogen chloride. The product was extracted with ether, the ether extract washed with brine and dried over magnesium sulfate, then concentrated in vacuo to give the title compound as a yellow liquid.
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