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[ CAS No. 4472-44-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4472-44-0
Chemical Structure| 4472-44-0
Structure of 4472-44-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4472-44-0 ]

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Product Citations

Product Details of [ 4472-44-0 ]

CAS No. :4472-44-0 MDL No. :MFCD00023199
Formula : C6H7ClN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RZVPFDOTMFYQHR-UHFFFAOYSA-N
M.W : 142.59 Pubchem ID :20550
Synonyms :

Calculated chemistry of [ 4472-44-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.97
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.76 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.04
Log Po/w (XLOGP3) : 1.98
Log Po/w (WLOGP) : 1.75
Log Po/w (MLOGP) : 0.89
Log Po/w (SILICOS-IT) : 2.42
Consensus Log Po/w : 1.82

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.46
Solubility : 0.489 mg/ml ; 0.00343 mol/l
Class : Soluble
Log S (Ali) : -2.15
Solubility : 1.02 mg/ml ; 0.00712 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.02
Solubility : 0.137 mg/ml ; 0.000959 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 4472-44-0 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4472-44-0 ]

* 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 [ 4472-44-0 ]

[ 4472-44-0 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 4472-44-0 ]
  • [ 124-41-4 ]
  • [ 14001-61-7 ]
  • 2
  • [ 4472-44-0 ]
  • [ 5131-60-2 ]
  • 1,3-bis(4,6-dimethyl-2-pyrimidyl)-4-chloro-1,3-phenylenediamine [ No CAS ]
  • 3
  • [ 4472-44-0 ]
  • [ 4637-24-5 ]
  • [ 14001-61-7 ]
  • [ 13012-25-4 ]
  • [ 179009-28-0 ]
  • 4
  • [ 4472-44-0 ]
  • sodium-methylate solution [ No CAS ]
  • [ 14001-61-7 ]
  • 5
  • [ 4472-44-0 ]
  • [ 16490-02-1 ]
  • 6
  • [ 4472-44-0 ]
  • [ 30757-50-7 ]
  • [ 1379668-61-7 ]
  • 7
  • [ 67-56-1 ]
  • [ 4472-44-0 ]
  • [ 201230-82-2 ]
  • [ 27427-89-0 ]
YieldReaction ConditionsOperation in experiment
With palladium bis[bis(diphenylphosphino)ferrocene] dichloride; triethylamine; In acetonitrile; at 20 - 100℃;Inert atmosphere; [0586] Synthesis of methyl 4, 6-dimethylpyrimidine-2-carboxylate: [0587] To a stirred solution of 2-chloro-4, 6-dimethylpyrimidine (1 g, 7.05 mmol) in MeOH: CH3CN (4: 1, 20 mL) under argon atmosphere were added triethyl amine (1.98 mL, 14.02 mmol) and Pd(dppf)2Cl2 (1 g, 1.40 mmol) at room temperature; heated to 100 C and stirred for 20 h under CO pressure in steel bomb. The reaction was monitored by TLC; after completion of the reaction, the reaction mixture was filtered through celite and the filtrate was concentrated in vacuo to obtain the crude. The crude was purified through silica gel column chromatography using 30% EtOAc/ Hexanes to afford methyl 4,6-dimethylpyrimidine-2-carboxylate (400 mg, 34%) as an off- white solid. [0588] 1H-NMR (CDCI3, 400 MHz): delta 7.20 (s, 1H), 4.07 (s, 3H), 2.61 (s, 6H); LC-MS: 87.29%; 167.2 (M++l); (column: X-Bridge C-18, 50 3.0 mm, 3.5 mupiiota); RT 1.47 min. 0.05% Aq TFA: ACN; 0.8 mL/min); TLC: 30% EtOAc/ Hexanes (R 0.3).
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