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[ CAS No. 37535-51-6 ] {[proInfo.proName]}

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Chemical Structure| 37535-51-6
Chemical Structure| 37535-51-6
Structure of 37535-51-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 37535-51-6 ]

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Product Details of [ 37535-51-6 ]

CAS No. :37535-51-6 MDL No. :MFCD00237827
Formula : C8H10N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :PDRJLZDUOULRHE-ZETCQYMHSA-N
M.W : 166.18 Pubchem ID :2761499
Synonyms :

Calculated chemistry of [ 37535-51-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 43.3
TPSA : 76.21 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -9.05 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.94
Log Po/w (XLOGP3) : -2.44
Log Po/w (WLOGP) : 0.04
Log Po/w (MLOGP) : -2.67
Log Po/w (SILICOS-IT) : 0.35
Consensus Log Po/w : -0.76

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 0.49
Solubility : 519.0 mg/ml ; 3.13 mol/l
Class : Highly soluble
Log S (Ali) : 1.38
Solubility : 3990.0 mg/ml ; 24.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -1.49
Solubility : 5.44 mg/ml ; 0.0327 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.94

Safety of [ 37535-51-6 ]

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 [ 37535-51-6 ]

* 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 [ 37535-51-6 ]

[ 37535-51-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 24424-99-5 ]
  • [ 37535-51-6 ]
  • [ 71239-85-5 ]
  • 2
  • [ 71239-85-5 ]
  • [ 348619-79-4 ]
  • [ 37535-51-6 ]
YieldReaction ConditionsOperation in experiment
REFERENCE EXAMPLE 4 2-Amino-3-(2-pyridyl)-1-propanol (Compound A5) The title compound was obtained in a manner similar to that in Reference Examples 1 to 3 by using N-(tert-butoxycarbonyl)-beta-(2-pyridyl)-alpha-alanine as a starting material, which was derived from beta-(2-pyridyl)-alpha-alanine obtained by the method described in Bulletin Chemical Society Japan (Bull. Chem. Soc. Japan), 41, p.1634, 1968. 1H-NMR (270 MHz, CDCl3) delta 2.79 (dd, 1H, J=13.5, 7.6 Hz), 2.97 (dd, 1H, J=13.5, 5.6 Hz), 3.26 (m, 1H), 3.45 (m, 1H), 3.57 (dd, 1H, J=11.2, 4.3 Hz), 7.17-7.25 (m, 2H), 7.68 (dt, 1H, J=7.6, 2.0 Hz), 8.50 (d, 1H, J=5.0 Hz). FAB-MS: m/z 153 (M++1).
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