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[ CAS No. 1123-55-3 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1123-55-3
Chemical Structure| 1123-55-3
Chemical Structure| 1123-55-3
Structure of 1123-55-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1123-55-3 ]

CAS No. :1123-55-3 MDL No. :MFCD10566715
Formula : C7H6N2S Boiling Point : -
Linear Structure Formula :- InChI Key :ZWUIKHROIQRWGT-UHFFFAOYSA-N
M.W : 150.20 Pubchem ID :12479792
Synonyms :

Calculated chemistry of [ 1123-55-3 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.02
TPSA : 67.15 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.49
Log Po/w (XLOGP3) : 1.7
Log Po/w (WLOGP) : 1.89
Log Po/w (MLOGP) : 0.85
Log Po/w (SILICOS-IT) : 2.47
Consensus Log Po/w : 1.68

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.51
Solubility : 0.466 mg/ml ; 0.0031 mol/l
Class : Soluble
Log S (Ali) : -2.73
Solubility : 0.283 mg/ml ; 0.00188 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.59
Solubility : 0.384 mg/ml ; 0.00256 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.94

Safety of [ 1123-55-3 ]

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 [ 1123-55-3 ]

* 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 [ 1123-55-3 ]
  • Downstream synthetic route of [ 1123-55-3 ]

[ 1123-55-3 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 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
  • 2
  • [ 3970-41-0 ]
  • [ 1123-55-3 ]
Reference: [1] Yakugaku Zasshi, 1942, vol. 62, p. 47,51; dtsch. Ref. S. 19, 22[2] Chem.Abstr., 1951, p. 609
[3] Phytochemistry, 2012, vol. 74, p. 159 - 165
  • 3
  • [ 95-16-9 ]
  • [ 1123-55-3 ]
Reference: [1] Yakugaku Zasshi, 1942, vol. 62, p. 47,51; dtsch. Ref. S. 19, 22[2] Chem.Abstr., 1951, p. 609
[3] J. Gen. Chem. USSR (Engl. Transl.), 1960, vol. 30, p. 1394 - 1397[4] Zhurnal Obshchei Khimii, 1960, vol. 30, p. 1363 - 1366
  • 4
  • [ 149-30-4 ]
  • [ 1123-55-3 ]
Reference: [1] J. Gen. Chem. USSR (Engl. Transl.), 1960, vol. 30, p. 1394 - 1397[2] Zhurnal Obshchei Khimii, 1960, vol. 30, p. 1363 - 1366
  • 5
  • [ 1123-55-3 ]
  • [ 767-70-4 ]
Reference: [1] Journal of the Chemical Society, 1965, p. 2248 - 2250
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