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[ CAS No. 1374652-22-8 ] {[proInfo.proName]}

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Chemical Structure| 1374652-22-8
Chemical Structure| 1374652-22-8
Structure of 1374652-22-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1374652-22-8 ]

CAS No. :1374652-22-8 MDL No. :MFCD22380551
Formula : C3H10Cl2N2O Boiling Point : -
Linear Structure Formula :- InChI Key :VCIUOQVHKQLWNE-UHFFFAOYSA-N
M.W : 161.03 Pubchem ID :92132824
Synonyms :

Calculated chemistry of [ 1374652-22-8 ]

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 34.95
TPSA : 47.28 Ų

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 : Yes
Log Kp (skin permeation) : -7.04 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.34
Log Po/w (WLOGP) : 0.45
Log Po/w (MLOGP) : -0.23
Log Po/w (SILICOS-IT) : -0.41
Consensus Log Po/w : 0.03

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.99
Solubility : 16.6 mg/ml ; 0.103 mol/l
Class : Very soluble
Log S (Ali) : -0.9
Solubility : 20.4 mg/ml ; 0.127 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.19
Solubility : 249.0 mg/ml ; 1.55 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.56

Safety of [ 1374652-22-8 ]

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

Application In Synthesis of [ 1374652-22-8 ]

* 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 [ 1374652-22-8 ]

[ 1374652-22-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1698492-94-2 ]
  • [ 1374652-22-8 ]
YieldReaction ConditionsOperation in experiment
2.88 mmol With hydrogenchloride In 1,4-dioxane; methanol at 20℃; for 5h; 66 Oxetan-3-ylhydrazine hydrochloride General procedure: To a solution of Boc-protected hydrazine (1 .0 eq.) in MeOH (0.5 M) was added 4 N HCI in 1 ,4-dioxane (8.0 eq.) and the reaction was stirred at RT for 5 h. Diethyl ether was added and a precipitate formed which was collected by filtration to provide the desired hydrazine intermediate. Alternatively, the mixture was concentrated under reduced pressure and used as such.; Following general procedure G, tert-butyl N-(oxetan-3-ylamino)carbamate (3.84 mmol) gave the titledcompound (2.88 mmol) as a brown oil. 1H NMR (400 MHz, DMSO-d6, ): 3.81-3.71 (m, 2H), 3.61 -3.53(m, 2H), 3.25-3.19 (m, 1H)
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