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[ CAS No. 754-10-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 754-10-9
Chemical Structure| 754-10-9
Structure of 754-10-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 754-10-9 ]

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Product Details of [ 754-10-9 ]

CAS No. :754-10-9 MDL No. :MFCD00008011
Formula : C5H11NO Boiling Point : No data available
Linear Structure Formula :(CH3)3CCO(NH2) InChI Key :XIPFMBOWZXULIA-UHFFFAOYSA-N
M.W : 101.15 Pubchem ID :12957
Synonyms :

Calculated chemistry of [ 754-10-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 28.8
TPSA : 43.09 ?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) : -6.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.24
Log Po/w (XLOGP3) : 0.54
Log Po/w (WLOGP) : 0.52
Log Po/w (MLOGP) : 0.49
Log Po/w (SILICOS-IT) : -0.04
Consensus Log Po/w : 0.55

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.74
Solubility : 18.4 mg/ml ; 0.181 mol/l
Class : Very soluble
Log S (Ali) : -1.02
Solubility : 9.74 mg/ml ; 0.0963 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.6
Solubility : 25.2 mg/ml ; 0.249 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 754-10-9 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 754-10-9 ]

* 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 [ 754-10-9 ]

[ 754-10-9 ] Synthesis Path-Downstream   1~4

  • 1
  • cis-diamminediaquaplatinum(II) dinitrate [ No CAS ]
  • [ 754-10-9 ]
  • [ 2386-53-0 ]
  • [Pt4(NH3)8(pivalamidato)4](n-C12H25SO3)5 [ No CAS ]
  • 2
  • [ 754-10-9 ]
  • [ 823221-93-8 ]
  • N-[6-chloro-4-(trifluoromethyl)-3-pyridyl]-2,2-dimethyl-propanamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
15% With methanesulfonic acid(2-dicyclohexylphosphino-2?,4?,6?-triisopropyl-1,1?-biphenyl)[2-(2?-amino-1,1?-biphenyl)]palladium(II); potassium carbonate; In 1,4-dioxane; at 90 - 110℃; for 2.5h; Procedure for synthesis of N-[6-chloro-4-(trifluoromethyl)-3-pyridyl]-2,2-dimethyl- propanamide (Step 1) A mixture of <strong>[823221-93-8]5-bromo-2-chloro-4-(trifluoromethyl)pyridine</strong> (commercially available) (75 mg, 0.288 mmol), 2,2-dimethylpropanamide (32 mg, 0.317 mmol), XantPhos Pd G3 precatalyst (13 mg, - - 0.014 mmol), K2C03 (79 mg, 0.57 mmol) in 1 ,4-Dioxane (0.5 ml.) was heated at 90C for 0.5h and then 1 10C for 2h. Purification by reverse phase HPLC delivered product (14 mg, 15%). LC-MS: (positive ES MH+ 281 ).
15% With XantPhos Pd G3 precatalyst; potassium carbonate; In 1,4-dioxane; at 90 - 110℃; for 2.5h; A mixture of <strong>[823221-93-8]5-bromo-2-chloro-4-(trifluoromethyl)pyridine</strong> (commercially available) (75 mg, 0.288mmol), 2,2-dimethylpropanamide (32 mg, 0.317 mmol), XantPhos Pd G3 precatalyst (13 mg,0.0 14 mmol), K2C03 (79 mg, 0.57 mmol) in 1 ,4-Dioxane (0.5 mL) was heated at 90C for 0.5hand then 110C for 2h. Purification by reverse phase HPLC delivered product (14 mg, 15%). LC-MS: (positive ES MH+ 281).
  • 3
  • [ 754-10-9 ]
  • [ 766-85-8 ]
  • [ 56619-93-3 ]
  • 4
  • [ 754-10-9 ]
  • [ 98-56-6 ]
  • [ 25617-34-9 ]
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