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[ CAS No. 5952-92-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5952-92-1
Chemical Structure| 5952-92-1
Structure of 5952-92-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5952-92-1 ]

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Product Details of [ 5952-92-1 ]

CAS No. :5952-92-1 MDL No. :MFCD00159641
Formula : C5H6N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UPPPWUOZCSMDTR-UHFFFAOYSA-N
M.W : 126.11 Pubchem ID :643160
Synonyms :

Calculated chemistry of [ 5952-92-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 30.45
TPSA : 55.12 ?2

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) : -7.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.81
Log Po/w (XLOGP3) : -0.24
Log Po/w (WLOGP) : 0.12
Log Po/w (MLOGP) : -0.4
Log Po/w (SILICOS-IT) : -0.26
Consensus Log Po/w : 0.01

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.82
Solubility : 19.3 mg/ml ; 0.153 mol/l
Class : Very soluble
Log S (Ali) : -0.46
Solubility : 43.8 mg/ml ; 0.347 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.13
Solubility : 93.7 mg/ml ; 0.743 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.09

Safety of [ 5952-92-1 ]

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

Application In Synthesis of [ 5952-92-1 ]

* 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 [ 5952-92-1 ]

[ 5952-92-1 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 5952-92-1 ]
  • [ 18107-18-1 ]
  • [ 5952-93-2 ]
YieldReaction ConditionsOperation in experiment
76% With methanol; In hexanes; at 0℃; for 0.333333h; [00263] Step A: (Trimethylsilyl)diazomethane (12.0 niL, 24 mmol, 2.0M solution in hexanes) was added dropwise via an addition funnel to a cold (O0C) solution of 1 -methyl- IH- pyrazole-4-carboxylic acid (0.59 g, 4.7 mmol) in MeOH (20 mL). The reaction mixture was stirred for 20 minutes and then concentrated. The crude product was partitioned between ethyl acetate (100 mL) and water (50 mL). The organics were dried, filtered and concentrated. The crude product was purified by flash chromatography, eluting with hexanes/ethyl acetate (4:1) to give methyl 1 -methyl- lH-pyrazole-4-carboxylate (0.50 g, 3.6 mmol, 76% yield) as a solid, m/z (APCI-pos) M+l = 141.1.
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