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[ CAS No. 18677-48-0 ] {[proInfo.proName]}

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Chemical Structure| 18677-48-0
Chemical Structure| 18677-48-0
Structure of 18677-48-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 18677-48-0 ]

CAS No. :18677-48-0 MDL No. :MFCD01646188
Formula : C7H9NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :LPFKVVZTNDJALE-UHFFFAOYSA-N
M.W : 139.15 Pubchem ID :817733
Synonyms :

Calculated chemistry of [ 18677-48-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.22
TPSA : 31.35 ?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) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 0.79
Log Po/w (WLOGP) : 1.1
Log Po/w (MLOGP) : -0.13
Log Po/w (SILICOS-IT) : 1.32
Consensus Log Po/w : 1.0

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 : 4.28 mg/ml ; 0.0307 mol/l
Class : Very soluble
Log S (Ali) : -1.03
Solubility : 13.0 mg/ml ; 0.0935 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.25
Solubility : 0.779 mg/ml ; 0.0056 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.74

Safety of [ 18677-48-0 ]

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

Application In Synthesis of [ 18677-48-0 ]

* 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 [ 18677-48-0 ]

[ 18677-48-0 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 625-92-3 ]
  • [ 124-41-4 ]
  • [ 18677-48-0 ]
  • 2
  • [ 18677-48-0 ]
  • [ 93-59-4 ]
  • [ 18600-19-6 ]
  • 4
  • [ 2457-47-8 ]
  • [ 124-41-4 ]
  • [ 18677-48-0 ]
YieldReaction ConditionsOperation in experiment
Reaction of 3,5-dichloropyridine (CAS 2457-47-8) with sodium methoxide gives compound 1 ( J. Chem. Soc. B, 1967, 1211). Reaction of compound 1 with peroxybenzoic acid leads to compound 2 (Rec. Trav. Chim. Pays-Bas, 1955, 74, 1171). Reaction of compound 2 with a mixture of nitric and sulfuric acids affords compound 3 (Rec. Trav. Chim. Pays-Bas, 1955, 74, 1171). Reaction of compound 3 with sodium methoxide gives 2,3,5-trimethoxypyridine 1-oxide 3-3 (J. Heterocycl. Chem., 1987, 24, 59). II. Keratin Dyeing Composition Components
  • 5
  • [ 2457-47-8 ]
  • [ 18677-48-0 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; In 3,5-dimethoxypyridine; water; dimethyl sulfoxide; (a) 3,5-dimethoxy-pyridine 50 g of 3,5-dichloro-pyridine are dissolved in 250 ml dimethylsulfoxide. 15 g sodium methylate are added to this solution under stirring. It is stirred under exclusion of moisture at 60-80 C. 15 g sodium methylate are further added after each of 8 and 16 hours. After a total of 72 hours' stirring, the reaction mixture is reacted with a little water and shaked out with diethylether. The ether phase, after drying, is distilled in a vacuum, resulting in 24 g (51% of theoretical amount) of 3,5-dimethoxy-pyridine in the boiling range 90-120 C. at 1.6*103 Pa. The product is polluted with a small amount of 3-chloro-5-methoxypyridine. It can, however, be employed directly in the next stage for nitrification, since the chloro-compound is not dinitrified and therefore can easily be removed upon crystallization of the 3,5-dimethoxy-2,6-dinitro-pyridine.
  • 6
  • [ 18677-48-0 ]
  • [ 18600-15-2 ]
  • 9
  • [ 18677-48-0 ]
  • 3,5-dimethoxy-1,2-dihydro-pyridine [ No CAS ]
  • 10
  • [ 18677-48-0 ]
  • [ 78-83-1 ]
  • [ 23815-45-4 ]
  • [ 79-22-1 ]
  • [ 875152-71-9 ]
  • 6-(3,5-dimethoxy-benzyl)-5-isobutoxy-3-oxo-3,6-dihydro-2<i>H</i>-pyridine-1-carboxylic acid methyl ester [ No CAS ]
  • 4-(3,5-dimethoxy-benzyl)-5-isobutoxy-3-oxo-3,6-dihydro-2<i>H</i>-pyridine-1-carboxylic acid methyl ester [ No CAS ]
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