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[ CAS No. 19337-97-4 ] {[proInfo.proName]}

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Chemical Structure| 19337-97-4
Chemical Structure| 19337-97-4
Structure of 19337-97-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 19337-97-4 ]

CAS No. :19337-97-4 MDL No. :MFCD00006410
Formula : C8H7NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VUVORVXMOLQFMO-ONEGZZNKSA-N
M.W : 149.15 Pubchem ID :776396
Synonyms :

Calculated chemistry of [ 19337-97-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.91
TPSA : 50.19 ?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) : -6.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.15
Log Po/w (XLOGP3) : 0.8
Log Po/w (WLOGP) : 1.07
Log Po/w (MLOGP) : 0.31
Log Po/w (SILICOS-IT) : 1.18
Consensus Log Po/w : 0.9

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.54
Solubility : 4.3 mg/ml ; 0.0288 mol/l
Class : Very soluble
Log S (Ali) : -1.44
Solubility : 5.47 mg/ml ; 0.0367 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.47
Solubility : 5.07 mg/ml ; 0.034 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.86

Safety of [ 19337-97-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 19337-97-4 ]

* 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 [ 19337-97-4 ]

[ 19337-97-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 19337-97-4 ]
  • [ 120277-39-6 ]
YieldReaction ConditionsOperation in experiment
With 4-methyl-morpholine; sodium borohydrid; isobutyl chloroformate; In 1,2-dimethoxyethane; water; PREPARATION 5 Isobutyl chloroformate (4.4 ml) was added dropwise to a suspension of (E)-3-(3-pyridyl)acrylic acid (5.0 g) and N-methylmorpholine (4.05 ml) in 1,2-dimethoxyethane (50 ml) under -18° C. After being stirred at the same temperature for 0.5 hour, a solution of sodium borohydride (1.86 g) in water (10 ml) was added to the mixture all at once. The resulting mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate, and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixed solvent of hexane and ethyl acetate as eluent. The fractions containing the objective compound were collected and evaporated under reduced pressure to give (E)-3-(3-pyridyl)-2-propen-1-ol (1.0 g) as an oil. NMR (CDCl3, delta): 4.40 (2H, d, J=4.0Hz), 6.52 (1H, dt, J=4.0, 16.1Hz, trans), 6.65 (1H, d, J=16.1Hz, trans), 7.45 (1H, dd, J=5.6, 8.0Hz), 7.89 (1H, d, J=8.0Hz), 8.44 (1H, d, J=15.6Hz), 8.58 (1H, s)
  • 2
  • [ 19337-97-4 ]
  • [ 118420-23-8 ]
YieldReaction ConditionsOperation in experiment
palladium on activated carbon; In N-methyl-acetamide; methanol; Reference Example 12 Preparation of 3-(3-pyridyl)propionic acid: A mixture of 5.0 g of 3-(3-pyridyl)acrylic acid, 0.4 g of 10% palladium on activated carbon, 150 ml of methanol, and 50 ml of dimethylformamide is hydrogenated at room temperature and atmospheric pressure. After removal of the catalyst by filtration, the filtrate is concentrated to give 5.1 g of the title compound. 3-(6-Methyl-3-pyridyl)propionic acid is prepared in substantially the same manner as in Reference Example 12, using the corresponding starting materials.
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