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[ CAS No. 4869-46-9 ] {[proInfo.proName]}

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Chemical Structure| 4869-46-9
Chemical Structure| 4869-46-9
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Product Details of [ 4869-46-9 ]

CAS No. :4869-46-9 MDL No. :MFCD00099582
Formula : C7H8N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :KGJFRZOATIXYPW-UHFFFAOYSA-N
M.W : 168.15 Pubchem ID :453092
Synonyms :

Calculated chemistry of [ 4869-46-9 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.87
TPSA : 61.07 Ų

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) : -7.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.41
Log Po/w (XLOGP3) : -0.94
Log Po/w (WLOGP) : -1.1
Log Po/w (MLOGP) : -0.98
Log Po/w (SILICOS-IT) : 0.11
Consensus Log Po/w : -0.3

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.59
Solubility : 42.8 mg/ml ; 0.254 mol/l
Class : Very soluble
Log S (Ali) : 0.14
Solubility : 233.0 mg/ml ; 1.39 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.53
Solubility : 49.3 mg/ml ; 0.293 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.73

Safety of [ 4869-46-9 ]

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 [ 4869-46-9 ]

* 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.

  • Upstream synthesis route of [ 4869-46-9 ]
  • Downstream synthetic route of [ 4869-46-9 ]

[ 4869-46-9 ] Synthesis Path-Upstream   1~12

  • 1
  • [ 1195-08-0 ]
  • [ 74-88-4 ]
  • [ 4869-46-9 ]
YieldReaction ConditionsOperation in experiment
89% With sodium hydride In DMF (N,N-dimethylformamide) at 20℃; for 0.5 h; To a slurry of 400mg of 5-formyluracil (2.8 mM) in DMF (10 mL) at room temperature was added sodium hydride (280 mg, 7 mM, 60percent in oil).
After stirring for 30 min., MeI (1.013 g, 7.2 mM) was added.
When the turbid reaction mixture became a homogeneous yellow solution tlc revealed the absence of starting uracil.
The reaction mixture was treated with MeOH and water, concentrated on the rotovap and the residue partitioned between MeOH and hexane.
The MeOH fraction was concentrated and the residue partitioned between chloroform and water.
The organic phase dried (MgSO4), filtered and concentrated to give 420 mg (89percent yield) of 1,3-dimethyl-5-formyluracil as an off-white waxy solid. 1H-NMR (DMSO-d6), δ=9.82 (s, 1H), 8.52 (s, 1H), 3.43 (s, 3H), 3.2 (s, 3H). LC/MS; rt=0.34 mins. m/z=169, [M+H]+.
Reference: [1] Patent: US2006/19965, 2006, A1, . Location in patent: Page/Page column 22
[2] European Journal of Organic Chemistry, 2015, vol. 2015, # 30, p. 6624 - 6630
  • 2
  • [ 874-14-6 ]
  • [ 68-12-2 ]
  • [ 4869-46-9 ]
Reference: [1] Archiv der Pharmazie, 1991, vol. 324, # 4, p. 203 - 207
[2] Journal of Organic Chemistry, 1985, vol. 50, # 9, p. 1512 - 1516
[3] Tetrahedron, 2003, vol. 59, # 3, p. 341 - 352
[4] Journal of Heterocyclic Chemistry, 2009, vol. 46, # 6, p. 1280 - 1284
[5] Arkivoc, 2016, vol. 2017, # 2, p. 149 - 161
  • 3
  • [ 4401-71-2 ]
  • [ 107097-10-9 ]
  • [ 4869-46-9 ]
  • [ 14181-46-5 ]
Reference: [1] Chemistry Letters, 1986, p. 1319 - 1322
[2] Chemistry Letters, 1986, p. 1319 - 1322
[3] Bulletin of the Chemical Society of Japan, 1994, vol. 67, # 8, p. 2257 - 2264
  • 4
  • [ 49846-86-8 ]
  • [ 4869-46-9 ]
Reference: [1] Journal of the American Chemical Society, 1983, vol. 105, p. 963
[2] Journal of the American Chemical Society, 1980, vol. 102, p. 3948
  • 5
  • [ 4401-71-2 ]
  • [ 5176-82-9 ]
  • [ 23450-35-3 ]
  • [ 38645-23-7 ]
  • [ 4869-46-9 ]
Reference: [1] Journal of Organic Chemistry, 1988, vol. 53, # 15, p. 3421 - 3424
[2] Journal of Organic Chemistry, 1988, vol. 53, # 15, p. 3421 - 3424
[3] Heterocycles, 1998, vol. 48, # 7, p. 1455 - 1459
[4] Heterocycles, 1998, vol. 48, # 7, p. 1455 - 1459
  • 6
  • [ 74226-50-9 ]
  • [ 4869-46-9 ]
Reference: [1] Journal of the American Chemical Society, 1980, vol. 102, p. 3948
[2] Journal of the American Chemical Society, 1983, vol. 105, p. 963
  • 7
  • [ 74226-51-0 ]
  • [ 4869-46-9 ]
Reference: [1] Journal of the American Chemical Society, 1980, vol. 102, p. 3948
[2] Journal of the American Chemical Society, 1983, vol. 105, p. 963
  • 8
  • [ 4401-71-2 ]
  • [ 66224-66-6 ]
  • [ 10320-84-0 ]
  • [ 107097-10-9 ]
  • [ 4869-46-9 ]
  • [ 14181-46-5 ]
Reference: [1] Chemistry Letters, 1990, # 7, p. 1105 - 1106
  • 9
  • [ 4401-71-2 ]
  • [ 66224-66-6 ]
  • [ 10320-84-0 ]
  • [ 130536-97-9 ]
  • [ 130536-96-8 ]
  • [ 107097-10-9 ]
  • [ 4869-46-9 ]
  • [ 14181-46-5 ]
Reference: [1] Chemistry Letters, 1990, # 7, p. 1105 - 1106
  • 10
  • [ 4401-71-2 ]
  • [ 4869-45-8 ]
  • [ 4869-46-9 ]
  • [ 14181-46-5 ]
Reference: [1] Journal of the Indian Chemical Society, 1997, vol. 74, # 1, p. 42 - 42
  • 11
  • [ 4401-71-2 ]
  • [ 23450-35-3 ]
  • [ 4869-45-8 ]
  • [ 38645-23-7 ]
  • [ 4869-46-9 ]
  • [ 14181-46-5 ]
Reference: [1] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1996, vol. 35, # 12, p. 1267 - 1270
  • 12
  • [ 4869-46-9 ]
  • [ 123-54-6 ]
  • [ 57009-12-8 ]
Reference: [1] Journal of Organic Chemistry, 1981, vol. 46, # 20, p. 3949 - 3953
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