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[ CAS No. 97004-04-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 97004-04-1
Chemical Structure| 97004-04-1
Structure of 97004-04-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 97004-04-1 ]

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Product Details of [ 97004-04-1 ]

CAS No. :97004-04-1 MDL No. :MFCD00673153
Formula : C6H7ClN2 Boiling Point : No data available
Linear Structure Formula :NH2CH2C5H3NCl InChI Key :XPARFBOWIYMLMY-UHFFFAOYSA-N
M.W : 142.59 Pubchem ID :7020927
Synonyms :

Calculated chemistry of [ 97004-04-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 36.92
TPSA : 38.91 ?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) : -6.69 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.39
Log Po/w (XLOGP3) : 0.67
Log Po/w (WLOGP) : 1.04
Log Po/w (MLOGP) : 0.49
Log Po/w (SILICOS-IT) : 1.61
Consensus Log Po/w : 1.04

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.57
Solubility : 3.81 mg/ml ; 0.0267 mol/l
Class : Very soluble
Log S (Ali) : -1.06
Solubility : 12.3 mg/ml ; 0.0864 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.66
Solubility : 0.311 mg/ml ; 0.00218 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 97004-04-1 ]

Signal Word:Danger Class:9
Precautionary Statements:P264-P273-P280-P280-P337+P313-P391 UN#:3077
Hazard Statements:H315-H318-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 97004-04-1 ]

* 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 [ 97004-04-1 ]

[ 97004-04-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 97004-04-1 ]
  • [ 53554-29-3 ]
  • ethyl 2-(((6-chloropyridin-3-yl)methyl)amino)-4-hydroxypyrimidine-5-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
77.8% In ethanol; for 24h;Reflux; Sealed tube; General procedure: To a Radley reaction carousel tube, add 1 equivalent 1, 1.1 equivalents of the amine, a stir bar, and 5 mL 95% ethanol. Reflux while stirring for 24 hours. After cooling to room temperature the resulting precipitate was collected by vacuum filtration, washing with 10 mL deionized water and 5 mL chloroform.
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