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[ CAS No. 2942-05-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 2942-05-4
Chemical Structure| 2942-05-4
Chemical Structure| 2942-05-4
Structure of 2942-05-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 2942-05-4 ]

CAS No. :2942-05-4 MDL No. :MFCD18451392
Formula : C7H4N2O2S Boiling Point : -
Linear Structure Formula :- InChI Key :HOXHADJRCXTPMR-UHFFFAOYSA-N
M.W : 180.18 Pubchem ID :298491
Synonyms :

Calculated chemistry of [ 2942-05-4 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 48.44
TPSA : 86.95 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.28
Log Po/w (XLOGP3) : 2.21
Log Po/w (WLOGP) : 2.2
Log Po/w (MLOGP) : 1.13
Log Po/w (SILICOS-IT) : 0.96
Consensus Log Po/w : 1.56

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.84
Solubility : 0.261 mg/ml ; 0.00145 mol/l
Class : Soluble
Log S (Ali) : -3.67
Solubility : 0.0385 mg/ml ; 0.000214 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.35
Solubility : 0.805 mg/ml ; 0.00447 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.34

Safety of [ 2942-05-4 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P270-P301+P312-P330-P501 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2942-05-4 ]

* 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.

  • Upstream synthesis route of [ 2942-05-4 ]
  • Downstream synthetic route of [ 2942-05-4 ]

[ 2942-05-4 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 95-16-9 ]
  • [ 2942-05-4 ]
  • [ 2942-08-7 ]
  • [ 2942-06-5 ]
Reference: [1] J. Gen. Chem. USSR (Engl. Transl.), 1960, vol. 30, p. 1394 - 1397[2] Zhurnal Obshchei Khimii, 1960, vol. 30, p. 1363 - 1366
  • 2
  • [ 95-16-9 ]
  • [ 2942-05-4 ]
  • [ 2942-06-5 ]
Reference: [1] Journal of the Chemical Society, 1954, p. 2261,2262
[2] Yakugaku Zasshi, 1952, vol. 72, p. 1266[3] Chem.Abstr., 1953, p. 12357
[4] Yakugaku Zasshi, 1942, vol. 62, p. 47,51; dtsch. Ref. S. 19, 22[5] Chem.Abstr., 1951, p. 609
  • 3
  • [ 2942-05-4 ]
  • [ 1123-55-3 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980, p. 2358 - 2361
[2] Yakugaku Zasshi, 1942, vol. 62, p. 47,51; dtsch. Ref. S. 19, 22[3] Chem.Abstr., 1951, p. 609
[4] J. Gen. Chem. USSR (Engl. Transl.), 1960, vol. 30, p. 1394 - 1397[5] Zhurnal Obshchei Khimii, 1960, vol. 30, p. 1363 - 1366
[6] Patent: WO2005/28445, 2005, A2, . Location in patent: Page/Page column 41-42
[7] Phytochemistry, 2012, vol. 74, p. 159 - 165
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