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[ CAS No. 4027-57-0 ] {[proInfo.proName]}

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Chemical Structure| 4027-57-0
Chemical Structure| 4027-57-0
Structure of 4027-57-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4027-57-0 ]

CAS No. :4027-57-0 MDL No. :MFCD00233455
Formula : C7H10N2O2 Boiling Point : No data available
Linear Structure Formula :C3H2N2(CH3)COOCH2CH3 InChI Key :BOTXQJAHRCGJEG-UHFFFAOYSA-N
M.W : 154.17 Pubchem ID :77645
Synonyms :
Chemical Name :Ethyl 5-methylpyrazole-3-carboxylate

Calculated chemistry of [ 4027-57-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.43
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.64
TPSA : 54.98 ?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) : -6.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.57
Log Po/w (XLOGP3) : 1.17
Log Po/w (WLOGP) : 0.89
Log Po/w (MLOGP) : 0.33
Log Po/w (SILICOS-IT) : 1.52
Consensus Log Po/w : 1.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.67
Solubility : 3.29 mg/ml ; 0.0213 mol/l
Class : Very soluble
Log S (Ali) : -1.92
Solubility : 1.85 mg/ml ; 0.012 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.09
Solubility : 1.26 mg/ml ; 0.00817 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.98

Safety of [ 4027-57-0 ]

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

Application In Synthesis of [ 4027-57-0 ]

* 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.

  • Upstream synthesis route of [ 4027-57-0 ]
  • Downstream synthetic route of [ 4027-57-0 ]

[ 4027-57-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 4027-57-0 ]
  • [ 6076-14-8 ]
YieldReaction ConditionsOperation in experiment
79% With N-Bromosuccinimide In N,N-dimethyl-formamide at 20℃; for 16 h; A mixture of ethyl 5-methyl-1H-pyrazole-3-carboxylate (4.0 g, 25.95 mmol) and NBS (5.08 g, 28.54 mmol) in N,N-dimethylformamide (15 mL) was stirred at room temperature for 16 h. The mixture was taken up in EtOAc (200 mL) and the organics were washed with saturated brine solution. The organics were then separated and dried (Na2SO4) before concentrated to dryness. The crude was then purified by flash column chromatography (PE/EA=3/2) to give ethyl 4-bromo-5-methyl-1H-pyrazole-3-carboxylate (4.8 g, 79percent yield) as a white solid. LCMS (ESI): [M+H]+=234.9.
Reference: [1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 5, p. 2419 - 2430
[2] Patent: US2018/282282, 2018, A1, . Location in patent: Paragraph 1042; 1043
[3] Journal fuer Praktische Chemie (Leipzig), 1930, vol. <2>126, p. 150,165[4] Chemische Berichte, 1928, vol. 61, p. 2405
[5] Journal fuer Praktische Chemie (Leipzig), 1930, vol. <2>126, p. 150,165[6] Chemische Berichte, 1928, vol. 61, p. 2405
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