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[ CAS No. 1150561-67-3 ]

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Chemical Structure| 1150561-67-3
Chemical Structure| 1150561-67-3
Structure of 1150561-67-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1150561-67-3 ]

CAS No. :1150561-67-3 MDL No. :MFCD12026101
Formula : C14H19BO4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :262.11 g/mol Pubchem ID :-
Synonyms :

Calculated chemistry of [ 1150561-67-3 ]

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 74.84
TPSA : 55.76 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.8
Log Po/w (WLOGP) : 1.99
Log Po/w (MLOGP) : 1.54
Log Po/w (SILICOS-IT) : 1.76
Consensus Log Po/w : 1.62

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.85

Water Solubility

Log S (ESOL) : -3.33
Solubility : 0.122 mg/ml ; 0.000467 mol/l
Class : Soluble
Log S (Ali) : -3.63
Solubility : 0.0618 mg/ml ; 0.000236 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.76
Solubility : 0.0455 mg/ml ; 0.000174 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.01

Safety of [ 1150561-67-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1150561-67-3 ]

* 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 [ 1150561-67-3 ]

[ 1150561-67-3 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 1150561-67-3 ]
  • [ 1628150-78-6 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride In chloroform; N,N-dimethyl-formamide at 20 - 35℃; 8.1 Synthesis of 3 -methyl-5-(4,4.5 ,5 ,-tetramethyl- 1,3 ,2-dioxaborolan-2-yl)benzoyl chloride: 3 -M ethyl-5 -(4,4,5,5 -tetramethyl- [1,3 ,2dioxaborolan-2-yl)-benzoic acid (700 mg. 2.67 mmol) was placed into 100 ml round bottom flask equipped with a stir bar. 3.0 ml of anhydrous chloroform was added to the flask followed by 2.0 ml of thionyl chloride and 1 drop of anhydrous DMF. Tiie reaction mixture was stirred at 35°C for 3 hours and then at room temperature overnight. LCMS of the sample after quenching a small amount with MeOH showed that no acid left. The solvent and excess thionyl chloride was removed under vacuum to give SKC-03-071. SKC-03-O7lwas used in the next step wthout further purification.
  • 2
  • [ 1150561-67-3 ]
  • [ 1628150-82-2 ]
  • [ 1628150-84-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: thionyl chloride / N,N-dimethyl-formamide; chloroform / 20 - 35 °C 2: triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere
  • 3
  • [ 1150561-67-3 ]
  • [ 1628150-84-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: thionyl chloride / N,N-dimethyl-formamide; chloroform / 20 - 35 °C 2.1: triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere 2.2: 2 h / 20 °C
YieldReaction ConditionsOperation in experiment
93% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In 1,4-dioxane at 110℃; Inert atmosphere; p General procedure: To a degassed souDon of 1,4-doxane (0.1 M), under an atmosphere of ntrogen,was addedthe benzoc acid (1 eq.), bs(pnacoato)dthoron (1 .5 eq.), and KOAc (4.4 eq.) sequenUafly.The mixture was degassed once again and then PdC2(dppf) (5 mo%) was added. Theresutng souUon was heated to 110°C overnight. The sovent was removed in vacuo to givea dark gummy residue, which was taken up nto EtOAc and H20. The organic ayer was separated and the aqueous was further extracted with EtOAc (2x). The combined organic ayers were washed with 2 M HC, dried over MgSO4 and concentrated in vacuo to give a dark brown sohd. The resutng sohd was trtu rated wth petroeum benzne to afford the Uflecompound. The foHowng compounds were made by the 8uzuk couphng method E
Historical Records

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