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[ CAS No. 20570-96-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 20570-96-1
Chemical Structure| 20570-96-1
Structure of 20570-96-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 20570-96-1 ]

CAS No. :20570-96-1 MDL No. :MFCD00012921
Formula : C7H12Cl2N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MSJHOJKVMMEMNX-UHFFFAOYSA-N
M.W : 195.09 Pubchem ID :146540
Synonyms :

Calculated chemistry of [ 20570-96-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 48.62
TPSA : 38.05 ?2

Pharmacokinetics

GI absorption : Low
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) : -5.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.38
Log Po/w (WLOGP) : -5.27
Log Po/w (MLOGP) : 2.07
Log Po/w (SILICOS-IT) : 0.67
Consensus Log Po/w : -0.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.82
Solubility : 0.295 mg/ml ; 0.00151 mol/l
Class : Soluble
Log S (Ali) : -2.82
Solubility : 0.295 mg/ml ; 0.00151 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.45
Solubility : 0.695 mg/ml ; 0.00356 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 20570-96-1 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P310+P330-P405 UN#:2811
Hazard Statements:H301-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 20570-96-1 ]

* 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 [ 20570-96-1 ]

[ 20570-96-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1194-21-4 ]
  • [ 20570-96-1 ]
  • [ 67873-25-0 ]
YieldReaction ConditionsOperation in experiment
67% With triethylamine; In water; (III) (R1 =CH2 C6 H5; X=O) A mixture of <strong>[1194-21-4]6-chloroisocytosine</strong> (17.50 g), triethylamine (90.10 g), and benzylhydrazine dihydrochloride (46.90 g) in water (900 ml) was refluxed for 10 minutes after which time the resulting solution was filtered to remove impurities present in the hydrazine salt. After refluxing the filtrate for 9 hours a white solid was collected by filtration from the hot reaction mixture, washed with water (250 ml) and dried overnight at room temperature in a vacuum desiccator protected from the light to yield 6-(1-benzylhydrazino)isocytosine (18.65 g; 67percent of theoretical yield, M.P. 270°-290° C. decomposition). Elemental analysis: Calcd. for C11 H13 N5 O: C 57.13percent, H 5.67percent, N 30.29percent. Found: C 57.15percent, H5.75percent, N30.25percent. NMR (DMSO-d6) delta4.34(br s,2H), 4.81(s,2H), 5.07 (s,1H),6.20 (br s,2H), 7.25 (s,5H), 9.80 (br s,1H).
  • 2
  • [ 20570-96-1 ]
  • [ 121358-86-9 ]
  • [ 1050619-85-6 ]
  • [ 1050619-79-8 ]
  • [ 1050619-74-3 ]
  • 3
  • [ 20570-96-1 ]
  • [ 151229-84-4 ]
  • 3-amino-1-benzyl-6-chloro-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile [ No CAS ]
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