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[ CAS No. 92534-69-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 92534-69-5
Chemical Structure| 92534-69-5
Structure of 92534-69-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 92534-69-5 ]

CAS No. :92534-69-5 MDL No. :MFCD00222738
Formula : C5H5N3O4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ANGMMUPJSXUXGY-UHFFFAOYSA-N
M.W : 171.11 Pubchem ID :592623
Synonyms :

Calculated chemistry of [ 92534-69-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.2
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.27
TPSA : 100.94 ?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) : -7.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.43
Log Po/w (XLOGP3) : -0.08
Log Po/w (WLOGP) : 0.03
Log Po/w (MLOGP) : -1.37
Log Po/w (SILICOS-IT) : -2.29
Consensus Log Po/w : -0.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.03
Solubility : 16.1 mg/ml ; 0.094 mol/l
Class : Very soluble
Log S (Ali) : -1.59
Solubility : 4.42 mg/ml ; 0.0258 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.45
Solubility : 486.0 mg/ml ; 2.84 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.96

Safety of [ 92534-69-5 ]

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

Application In Synthesis of [ 92534-69-5 ]

* 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 [ 92534-69-5 ]
  • Downstream synthetic route of [ 92534-69-5 ]

[ 92534-69-5 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 67-56-1 ]
  • [ 92534-69-5 ]
  • [ 309740-49-6 ]
YieldReaction ConditionsOperation in experiment
83% for 16 h; Heating / reflux [0227] To a solution of l-methyl-4-nitro-lH-pyrazole-5-carboxylic acid (2 g, for the synthesis of l-methyl-4-nitro-lH-pyrazole-5-carboxylic acid, see Perevalov, V. P., et. al.; Chem. Het. Compounds 19; 12; 1983; 1326-1330) in methanol (20 mL), was added HCl (g). The resulting solution was allowed to react, with stirring, for 16 h at reflux. The mixture was concentrated to give methyl l-methyl-4-nitro-lH-pyrazole-5- carboxylate as a yellow oil (1.8 g, 83percent). LCMS: 185 (M+H) +. Step 2: Methyl 4-amino-l-methyl-lH-pyrazole-5-carboxylate
Reference: [1] Patent: WO2009/26241, 2009, A1, . Location in patent: Page/Page column 66-67
  • 2
  • [ 77-78-1 ]
  • [ 400877-57-8 ]
  • [ 309740-49-6 ]
  • [ 92534-69-5 ]
Reference: [1] Tetrahedron Letters, 2009, vol. 50, # 22, p. 2624 - 2627
  • 3
  • [ 3185-99-7 ]
  • [ 400877-57-8 ]
  • [ 309740-49-6 ]
  • [ 92534-69-5 ]
  • [ 4598-86-1 ]
Reference: [1] Tetrahedron Letters, 2009, vol. 50, # 22, p. 2624 - 2627
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