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[ CAS No. 1570-48-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1570-48-5
Chemical Structure| 1570-48-5
Structure of 1570-48-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1570-48-5 ]

CAS No. :1570-48-5 MDL No. :MFCD00023589
Formula : C8H9NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :VDNKJMUNLKAGAM-UHFFFAOYSA-N
M.W : 135.16 Pubchem ID :74074
Synonyms :

Calculated chemistry of [ 1570-48-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 39.24
TPSA : 29.96 ?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) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.57
Log Po/w (XLOGP3) : 0.9
Log Po/w (WLOGP) : 1.67
Log Po/w (MLOGP) : 0.46
Log Po/w (SILICOS-IT) : 1.98
Consensus Log Po/w : 1.32

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.56
Solubility : 3.75 mg/ml ; 0.0277 mol/l
Class : Very soluble
Log S (Ali) : -1.11
Solubility : 10.4 mg/ml ; 0.0769 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.73
Solubility : 0.25 mg/ml ; 0.00185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.26

Safety of [ 1570-48-5 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1570-48-5 ]

* 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 [ 1570-48-5 ]

[ 1570-48-5 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 1570-48-5 ]
  • [ 60289-67-0 ]
YieldReaction ConditionsOperation in experiment
Precursor 3 n: 1-Pyridin-3-yl-propylamine 0.9 g of the title compound was obtained from 1 g of 3-propionylpyridine according to general method 3 B. Precursor 3 s: 1-Cyclopropyl-1-phenylmethylamine Hydrochloride
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