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[ CAS No. 1464025-91-9 ] {[proInfo.proName]}

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Chemical Structure| 1464025-91-9
Chemical Structure| 1464025-91-9
Structure of 1464025-91-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1464025-91-9 ]

CAS No. :1464025-91-9 MDL No. :MFCD27920593
Formula : C21H40N2O5 Boiling Point : -
Linear Structure Formula :- InChI Key :BBZZIJOSFVOUGF-LOLRQIBTSA-N
M.W : 400.55 Pubchem ID :73554152
Synonyms :

Calculated chemistry of [ 1464025-91-9 ]

Physicochemical Properties

Num. heavy atoms : 28
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 8
Num. H-bond acceptors : 6.0
Num. H-bond donors : 4.0
Molar Refractivity : 111.2
TPSA : 107.89 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.33
Log Po/w (XLOGP3) : 1.44
Log Po/w (WLOGP) : 3.59
Log Po/w (MLOGP) : 1.9
Log Po/w (SILICOS-IT) : 2.99
Consensus Log Po/w : 2.65

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.7
Solubility : 0.794 mg/ml ; 0.00198 mol/l
Class : Soluble
Log S (Ali) : -3.31
Solubility : 0.196 mg/ml ; 0.000488 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.8
Solubility : 0.629 mg/ml ; 0.00157 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 4.26

Safety of [ 1464025-91-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1464025-91-9 ]

* 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 [ 1464025-91-9 ]

[ 1464025-91-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 446-34-4 ]
  • [ 1464025-91-9 ]
  • [ 1562189-33-6 ]
YieldReaction ConditionsOperation in experiment
53.6% Step 1 : In a similar manner to that described for the preparation of (S)-2-(tert- butoxycarbonylamino)-3-(5-methyl-2-nitrophenoxy)propanoic acid except the reaction mixture was stirred at 0 C for 4 h, <strong>[1464025-91-9](2S,3S)-2-(tert-butoxycarbonylamino)-3-hydroxybutanoic acid DCHA</strong> (2.0 g, 5.00 mmol) and 2-fluoro-4-methyl-l -nitrobenzene (1.55 g, 9.99 mmol) were converted to (2S,3S)-2-tert-butoxycarbonylamino-3-(5-methyl-2-nitro-phenoxy)-butyric acid (0.95 g, 53.6 % yield).
  • 2
  • [ 1464025-91-9 ]
  • [ 1562189-39-2 ]
  • 3
  • [ 367-86-2 ]
  • [ 1464025-91-9 ]
  • C16H19F3N2O7 [ No CAS ]
YieldReaction ConditionsOperation in experiment
(2S,3S)-3-Amino-2-methyl-7-(trifluoromethyl)-2,3-dihydrobenzo[b][l,4]oxazepin- 4(5H)-one trifluoroacetate In a similar manner to that described for the preparation of (S)-3-amino-8-methyl-2,3- dihydrobenzo[b][l,4]oxazepin-4(5H)-one trifluoroacetate except in Step 1 the mixture was stirred overnight and in Step 2 the mixture was stirred 3 h, (2S,3S)-2-(tert- butoxycarbonylamino)-3-hydroxybutanoic acid discyclohexylamine salt (2.0 g, 5.00 mmol) and l-fluoro-2-nitro-4-(trifluoromethyl)benzene (1.04 g, 5.00 mmol) were converted to the title compound (58 mg) which was used without purification.
  • 4
  • [ 367-86-2 ]
  • [ 1464025-91-9 ]
  • C16H21F3N2O5 [ No CAS ]
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