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[ CAS No. 70918-54-6 ] {[proInfo.proName]}

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Chemical Structure| 70918-54-6
Chemical Structure| 70918-54-6
Structure of 70918-54-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 70918-54-6 ]

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Product Details of [ 70918-54-6 ]

CAS No. :70918-54-6 MDL No. :MFCD00239408
Formula : C9H8O4 Boiling Point : -
Linear Structure Formula :- InChI Key :HMBHAQMOBKLWRX-QMMMGPOBSA-N
M.W : 180.16 Pubchem ID :687061
Synonyms :

Calculated chemistry of [ 70918-54-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.89
TPSA : 55.76 ?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) : -6.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.34
Log Po/w (XLOGP3) : 1.4
Log Po/w (WLOGP) : 0.91
Log Po/w (MLOGP) : 0.4
Log Po/w (SILICOS-IT) : 1.08
Consensus Log Po/w : 1.02

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.11
Solubility : 1.38 mg/ml ; 0.00768 mol/l
Class : Soluble
Log S (Ali) : -2.17
Solubility : 1.2 mg/ml ; 0.00668 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.57
Solubility : 4.84 mg/ml ; 0.0269 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.75

Safety of [ 70918-54-6 ]

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 [ 70918-54-6 ]

* 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 [ 70918-54-6 ]

[ 70918-54-6 ] Synthesis Path-Downstream   1~12

  • 1
  • 1,4-benzodioxane-2-carboxylic acid [ No CAS ]
  • [ 70918-54-6 ]
  • 2
  • [ 541-41-3 ]
  • [ 70918-54-6 ]
  • C12H12O6 [ No CAS ]
  • 3
  • [ 251104-21-9 ]
  • [ 70918-54-6 ]
  • 4
  • [ 4739-94-0 ]
  • [ 70918-54-6 ]
  • (R)-ethyl 2,3-dihydrobenzo[b][1,4]dioxine-2-carboxylate [ No CAS ]
  • 5
  • [ 70918-54-6 ]
  • [ 401947-96-4 ]
YieldReaction ConditionsOperation in experiment
100% With thionyl chloride; In toluene; at 0℃; under 760.051 Torr; for 4h;Reflux; General procedure: Thionyl chloride (4 eq) was added dropwise at 0 C to a solutionof (R)- or <strong>[70918-54-6](S)-2,3-dihydro-benzo[1,4]dioxine-2-carboxylic acid</strong> (1eq) in toluene (5 mL). The mixture was stirred at reflux for 4 h. Thesolvent was then evaporated to dryness affording 13 and 14,respectively, as a yellow oil in quantitative yield.
  • 6
  • [ 67-56-1 ]
  • [ 70918-54-6 ]
  • (S)‐methyl 1,4‐benzodioxane‐2‐carboxylate [ No CAS ]
  • 7
  • 1,4-benzodioxane-2-carboxylic acid [ No CAS ]
  • [ 70918-54-6 ]
  • [ 70918-53-5 ]
  • 8
  • [ 120-80-9 ]
  • [AlO4Al12(OH)24(H2O)12]7+ [ No CAS ]
  • [ 70918-54-6 ]
  • 11
  • [ 70918-54-6 ]
  • (+)-Doxazosin hydrochloride [ No CAS ]
  • 12
  • [ 70918-54-6 ]
  • (+)-(S)-doxazosin mesylate [ No CAS ]
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