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[ CAS No. 1076-96-6 ] {[proInfo.proName]}

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Chemical Structure| 1076-96-6
Chemical Structure| 1076-96-6
Structure of 1076-96-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1076-96-6 ]

CAS No. :1076-96-6 MDL No. :MFCD00017218
Formula : C10H10O2 Boiling Point : No data available
Linear Structure Formula :CH2CHC6H4CO2CH3 InChI Key :NUMHUJZXKZKUBN-UHFFFAOYSA-N
M.W : 162.19 Pubchem ID :583124
Synonyms :

Calculated chemistry of [ 1076-96-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.1
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.81
TPSA : 26.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.08 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.37
Log Po/w (XLOGP3) : 3.11
Log Po/w (WLOGP) : 2.01
Log Po/w (MLOGP) : 2.47
Log Po/w (SILICOS-IT) : 2.5
Consensus Log Po/w : 2.49

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.98
Solubility : 0.171 mg/ml ; 0.00105 mol/l
Class : Soluble
Log S (Ali) : -3.33
Solubility : 0.0757 mg/ml ; 0.000467 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.91
Solubility : 0.2 mg/ml ; 0.00123 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.49

Safety of [ 1076-96-6 ]

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

Application In Synthesis of [ 1076-96-6 ]

* 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 [ 1076-96-6 ]

[ 1076-96-6 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 1076-96-6 ]
  • [ 3609-53-8 ]
  • [ 84851-56-9 ]
  • 2
  • [ 1076-96-6 ]
  • [ 3609-53-8 ]
  • [ 84851-56-9 ]
  • [ 143687-55-2 ]
  • 3
  • [ 6018-41-3 ]
  • [ 1076-96-6 ]
  • [ 792-74-5 ]
  • 5
  • [ 1076-96-6 ]
  • [ 84851-56-9 ]
  • 6
  • [ 24424-99-5 ]
  • [ 676593-23-0 ]
  • [ 74-88-4 ]
  • [ 1076-96-6 ]
YieldReaction ConditionsOperation in experiment
74% General procedure: A 15 mL Schlenk tube equipped with a stirrer bar was chargedwith CuCl (10 mol%), L7 (13 mol%), LiOMe (2.5 equiv), and theappropriate boronic ester 1 or 4 (0.375 mmol). The vessel wasthen evacuated and filled with Ar (three cycles). DMA (0.5 mL)and (Boc)2O (0.25 mmol) were added sequentially under Ar, andthe mixture was stirred at 30 for 6 h. MeI (5 equiv) was thenadded in air, and the mixture was stirred at 30 for additional2 h. The mixture was finally diluted with EtOAc and washedwith sat. aq NaCl (20 mL). The aqueous phase was furtherextracted with EtOAc (3 × 20 mL), and the combined organicphases were dried (Na2SO4) and concentrated. The residue waspurified by column chromatography [silica gel EtOAc-hexane(1:100 to 1:50)].
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