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[ CAS No. 23788-74-1 ] {[proInfo.proName]}

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Chemical Structure| 23788-74-1
Chemical Structure| 23788-74-1
Structure of 23788-74-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 23788-74-1 ]

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Product Details of [ 23788-74-1 ]

CAS No. :23788-74-1 MDL No. :MFCD00063233
Formula : C13H18O5S Boiling Point : -
Linear Structure Formula :CH3C6H4SO3CH2C3H3O2(CH3)2 InChI Key :SRKDUHUULIWXFT-LLVKDONJSA-N
M.W : 286.34 Pubchem ID :6993835
Synonyms :

Calculated chemistry of [ 23788-74-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.54
Num. rotatable bonds : 4
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 69.72
TPSA : 70.21 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.75 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.77
Log Po/w (XLOGP3) : 1.83
Log Po/w (WLOGP) : 2.93
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 1.86
Consensus Log Po/w : 2.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.74
Solubility : 0.524 mg/ml ; 0.00183 mol/l
Class : Soluble
Log S (Ali) : -2.92
Solubility : 0.341 mg/ml ; 0.00119 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.69
Solubility : 0.0579 mg/ml ; 0.000202 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.81

Safety of [ 23788-74-1 ]

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 [ 23788-74-1 ]

* 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 [ 23788-74-1 ]

[ 23788-74-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 272-97-9 ]
  • [ 23788-74-1 ]
  • 7-(S)-(2,2-dimethyl-1,3-dioxolan-4-yl)methyl-3-deazapurine [ No CAS ]
  • 9-(S)-(2,2-dimethyl-1,3-dioxolan-4-yl)methyl-3-deazapurine [ No CAS ]
  • 2
  • [ 30818-28-1 ]
  • [ 23788-74-1 ]
  • [ 203259-53-4 ]
  • 3
  • [ 89942-77-8 ]
  • [ 23788-74-1 ]
  • methyl 3-((R)-2,2-dimethyl-1,3-dioxolan-4-ylmethyloxy)-2-nitrobenzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In 1-methyl-pyrrolidin-2-one; hexane; ethyl acetate; Step 2 To a solution of <strong>[89942-77-8]methyl <strong>[89942-77-8]3-hydroxy-2-nitrobenzoate</strong></strong> (1.97 g, 10 mmol) in N-methylpyrrolidinone (15 mL) was added (R)-2,2-dimethyl-1,3-dioxolan-4-ylmethyl p-tosylate (3.43 g, 1.2 eq.), and followed by K2CO3 (4.2 g, 3 eq.). After the mixture was heated at 96 C. overnight, was cooled to room temperature, quenched with H2O, and partitioned between H2O and EtOAc. The organic layer was separated, washed with H2O and NaCl (sat.), and then dried over Na2SO4. The crude product was purified on a silica gel column with 20% EtOAc in hexane to give methyl 3-((R)-2,2-dimethyl-1,3-dioxolan-4-ylmethyloxy)-2-nitrobenzoate as an oil (3.1 g).
  • 4
  • [ 68631-52-7 ]
  • [ 23788-74-1 ]
  • diethyl (S)-4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]pyridine-2,6-dicarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
82% With potassium carbonate; In N,N-dimethyl-formamide; at 70℃; for 96h; 4-Hydroxypyridine-2,6-dicarboxylate (0.50g, 2.09mmol), (R)-2,2-Dimethyl-1,3-dioxolane-4-methanol p-toluenesulfonate (0.72g, 2.5mmol) and potassium carbonate (1.03g, 7.45mmol) were suspended in anhydrous DMF (20mL). The mixture was stirred at 70C for 96h, after which it was evaporated to dryness. The residue was dissolved in CH2Cl2 (100mL) and washed with water (100mL). The organic layer was dried with Na2SO4 and evaporated to dryness. The crude product thus obtained was purified on a silica gel column eluting with a mixture of MeOH and CH2Cl2 (6:94, v/v). Yield 0.61g (82%). 1H-NMR (400MHz, CDCl3): 7.77 (s, 2H, Pyr-H3 & -H5), 4.48 (m, 1H, dioxolane-H5), 4.43 (q, J=7.1, 4H, CO2CH2CH3), 4.20-4.09 (m, 3H, dioxolane-H4 & PyrOCH2), (dd, J=5.8, 8.6, 1H, dioxolane-H4), 1.42 (s, 3H, dioxolane-CH3), 1.41 (t, J=7.1, 6H, CO2CH2CH3), 1.36 (s, 3H, dioxolane-CH3). 13C-NMR (100MHz, CDCl3): 166.5 (2C, CONH2), 164.5 (Pyr-C4), 150.3 (2C, Pyr-C2 & -C6), 114.3 (2C, Pyr-C3 & -C5), 110.1 (dioxolane-C2), 73.4 (dioxolane-C5), 69.3 (PyrOCH2), 66.3 (dioxolane-C4), 62.3 (2C, CO2CH2CH3), 26.7 (dioxolane-CH3), 25.2 (dioxolane-CH3), 14.2 (2C, CO2CH2CH3). HR-ESI-MS: 354.1547 ([M+H]+, C17H24NO7+; calc. 354.1547).
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