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[ CAS No. 52867-42-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 52867-42-2
Chemical Structure| 52867-42-2
Structure of 52867-42-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 52867-42-2 ]

CAS No. :52867-42-2 MDL No. :MFCD00459835
Formula : C6H8N2O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :IYAQFZAPKKWPNU-UHFFFAOYSA-N
M.W : 156.14 Pubchem ID :304501
Synonyms :

Calculated chemistry of [ 52867-42-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.33
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 37.59
TPSA : 64.09 ?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) : -7.3 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.36
Log Po/w (XLOGP3) : -0.07
Log Po/w (WLOGP) : -0.5
Log Po/w (MLOGP) : -0.13
Log Po/w (SILICOS-IT) : 0.34
Consensus Log Po/w : 0.2

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.97
Solubility : 16.8 mg/ml ; 0.108 mol/l
Class : Very soluble
Log S (Ali) : -0.82
Solubility : 23.4 mg/ml ; 0.15 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.77
Solubility : 26.7 mg/ml ; 0.171 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.86

Safety of [ 52867-42-2 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 52867-42-2 ]

* 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 [ 52867-42-2 ]

[ 52867-42-2 ] Synthesis Path-Downstream   1~11

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YieldReaction ConditionsOperation in experiment
23% In methanol; water; at 70℃; To a solution of dimethyl acetylenedicarboxylate (5 g, 35.18 mmol) in methanol (25 mL)-water (2.5mL) was added dropwise methylhydrazine (1.945 g, 42.22 mmol) at room temperature. The reaction mixture was stirred at 70C overnight, cooled to room temperature, concentrated under reduced pressure, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The obtained residue was purified by silica gel column chromatography [eluent: hexane-ethyl acetate (90:10-3:4)] to give the title compound (1.26 g) as a colorless oil (yield 23%). MS (ESI+): [M+H]+157. 1H NMR (300 MHz, DMSO-d6) delta 3.79 (3H, s), 3.88 (3H, s), 6.00 (1H, s), 10.06 (1H, s).
5 g In methanol; water; at 0 - 70℃; for 10h; The compound methyl hydrazine (10g) was dissolved in methanol (20mL) and water (10mL), cooled to 0 degree, stirred for 15min, then compound 21 (12g) was added dropwise to the reaction system, heated to 70 degrees for 10h, then the system temperature was returned to room temperature, the reaction 12h, filtered off with suction, the filter cake was washed with water (5mL), dried to give 22 as a pale yellow solid 5g
5 g In methanol; water; at 0 - 70℃; for 10.25h; The compound methyl hydrazine (10 g) was dissolved in methanol (20 mL) and water (10 mL).The temperature was lowered to 0 , stirred for 15 min, and then Compound 21 (12 g) was added dropwise to the reaction system.Heat to 70 for 10 h, then return the system temperature to room temperature.After 12 h of reaction, suction filtration, and the filter cake was washed with water (5 mL).Get 22 pale yellow solids 5g
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