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[ CAS No. 1269021-92-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1269021-92-2
Chemical Structure| 1269021-92-2
Structure of 1269021-92-2 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 1269021-92-2 ]

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Product Details of [ 1269021-92-2 ]

CAS No. :1269021-92-2 MDL No. :MFCD18483101
Formula : C8H16ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :GBEGAENNEGTOQG-UHFFFAOYSA-N
M.W : 193.67 Pubchem ID :53621921
Synonyms :

Calculated chemistry of [ 1269021-92-2 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.15
TPSA : 52.32 Ų

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) : -6.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.16
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 1.0
Log Po/w (SILICOS-IT) : 1.16
Consensus Log Po/w : 0.96

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.51
Solubility : 6.02 mg/ml ; 0.0311 mol/l
Class : Very soluble
Log S (Ali) : -1.85
Solubility : 2.71 mg/ml ; 0.014 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.49
Solubility : 6.25 mg/ml ; 0.0323 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.84

Safety of [ 1269021-92-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1269021-92-2 ]

* 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 [ 1269021-92-2 ]

[ 1269021-92-2 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 2384379-01-3 ]
  • [ 1269021-92-2 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride In dichloromethane; ethyl acetate at 20℃; for 1h; Inert atmosphere;
  • 3
  • [ 317829-98-4 ]
  • [ 1269021-92-2 ]
  • [ 2446325-87-5 ]
YieldReaction ConditionsOperation in experiment
Stage #1: ethyl 1-(aminomethyl)cyclobutanecarboxylate hydrochloride With triethylamine In methanol at 20℃; for 0.5h; Stage #2: 1-benzyloxycarbonyl-4-(tert-butyloxycarbonyl)piperazine-2-carboxaldehyde In methanol at 20℃; for 1h; Inert atmosphere; Stage #3: With sodium cyanoborohydride at 0 - 20℃; for 2h;
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