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[ CAS No. 56745-01-8 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 56745-01-8
Chemical Structure| 56745-01-8
Chemical Structure| 56745-01-8
Structure of 56745-01-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 56745-01-8 ]

CAS No. :56745-01-8 MDL No. :MFCD00504524
Formula : C5H3BrCl2N2 Boiling Point : -
Linear Structure Formula :- InChI Key :RRWAPFKBOJWJGU-UHFFFAOYSA-N
M.W : 241.90 Pubchem ID :4591837
Synonyms :

Calculated chemistry of [ 56745-01-8 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.72
TPSA : 25.78 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) : -5.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.27
Log Po/w (XLOGP3) : 3.22
Log Po/w (WLOGP) : 2.85
Log Po/w (MLOGP) : 1.92
Log Po/w (SILICOS-IT) : 3.35
Consensus Log Po/w : 2.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.81
Solubility : 0.0373 mg/ml ; 0.000154 mol/l
Class : Soluble
Log S (Ali) : -3.43
Solubility : 0.0891 mg/ml ; 0.000368 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.13
Solubility : 0.0179 mg/ml ; 0.0000741 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.86

Safety of [ 56745-01-8 ]

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 [ 56745-01-8 ]

* 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.

  • Upstream synthesis route of [ 56745-01-8 ]
  • Downstream synthetic route of [ 56745-01-8 ]

[ 56745-01-8 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 56745-01-8 ]
  • [ 3438-46-8 ]
Reference: [1] Journal of the American Chemical Society, 1954, vol. 76, p. 1953
  • 2
  • [ 56745-01-8 ]
  • [ 13036-57-2 ]
Reference: [1] Yakugaku Zasshi, 1950, vol. 70, p. 137[2] Chem.Abstr., 1950, p. 5886
  • 3
  • [ 56745-01-8 ]
  • [ 5424-21-5 ]
Reference: [1] Yakugaku Zasshi, 1950, vol. 70, p. 137[2] Chem.Abstr., 1950, p. 5886
  • 4
  • [ 56745-01-8 ]
  • [ 5541-07-1 ]
Reference: [1] Yakugaku Zasshi, 1942, vol. 62, p. 315,333; dtsch. Ref. S. 95, 106[2] Chem.Abstr., 1951, p. 5150
  • 5
  • [ 15018-56-1 ]
  • [ 56745-01-8 ]
Reference: [1] Journal of Heterocyclic Chemistry, 2006, vol. 43, # 5, p. 1327 - 1329
[2] Journal of the American Chemical Society, 1954, vol. 76, p. 1953
[3] Yakugaku Zasshi, 1950, vol. 70, p. 137[4] Chem.Abstr., 1950, p. 5886
[5] Yakugaku Zasshi, 1942, vol. 62, p. 315,333; dtsch. Ref. S. 95, 106[6] Chem.Abstr., 1951, p. 5150
[7] Journal of Coordination Chemistry, 2010, vol. 63, # 18, p. 3187 - 3197
[8] Journal of Medicinal Chemistry, 2011, vol. 54, # 2, p. 510 - 524
  • 6
  • [ 626-48-2 ]
  • [ 56745-01-8 ]
Reference: [1] Journal of Heterocyclic Chemistry, 2006, vol. 43, # 5, p. 1327 - 1329
[2] Yakugaku Zasshi, 1942, vol. 62, p. 315,333; dtsch. Ref. S. 95, 106[3] Chem.Abstr., 1951, p. 5150
  • 7
  • [ 6328-58-1 ]
  • [ 56745-01-8 ]
Reference: [1] Yakugaku Zasshi, 1950, vol. 70, p. 137[2] Chem.Abstr., 1950, p. 5886
  • 8
  • [ 33238-63-0 ]
  • [ 56745-01-8 ]
Reference: [1] Yakugaku Zasshi, 1950, vol. 70, p. 137[2] Chem.Abstr., 1950, p. 5886
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