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[ CAS No. 71441-76-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 71441-76-4
Chemical Structure| 71441-76-4
Structure of 71441-76-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 71441-76-4 ]

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Product Details of [ 71441-76-4 ]

CAS No. :71441-76-4 MDL No. :MFCD00001284
Formula : C7H12O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :IZPYNZLFBUQGCZ-UHFFFAOYSA-N
M.W : 128.17 Pubchem ID :544234
Synonyms :

Calculated chemistry of [ 71441-76-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 34.67
TPSA : 26.3 ?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) : -6.16 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.23
Log Po/w (XLOGP3) : 1.3
Log Po/w (WLOGP) : 1.29
Log Po/w (MLOGP) : 1.23
Log Po/w (SILICOS-IT) : 1.66
Consensus Log Po/w : 1.54

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.26
Solubility : 7.11 mg/ml ; 0.0555 mol/l
Class : Very soluble
Log S (Ali) : -1.45
Solubility : 4.52 mg/ml ; 0.0353 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.53
Solubility : 3.8 mg/ml ; 0.0296 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.29

Safety of [ 71441-76-4 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P270-P301+P312-P330 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 71441-76-4 ]

* 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 [ 71441-76-4 ]

[ 71441-76-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 71441-76-4 ]
  • [ 15910-91-5 ]
  • 2
  • [ 71441-76-4 ]
  • [ 72790-89-7 ]
YieldReaction ConditionsOperation in experiment
99% With hydrazine hydrate; In toluene; Reference Example 2 Preparation of 1-methyl-1-cyclopropanecarbohydrazide: A mixture of ethyl 1-methyl-1-cyclopropanecarboxylate (10 g, 7.8 mmole) and hydrazine monohydrate (5.1 g, 0.1 mole) is heated with stirring at 100° C. for 4 hours. To the reaction solution is added toluene (50 ml), and the mixture is refluxed for 3 hours while distilling off water. After cooling, the precipitated crystals are collected by filtration, and washed with diisopropyl ether to give the desired compound (8.9 g) as a colorless crystal. Yield: 99percent m.p. 85°-87° C.
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