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[ CAS No. 2683-35-4 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 2683-35-4
Chemical Structure| 2683-35-4
Chemical Structure| 2683-35-4
Structure of 2683-35-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 2683-35-4 ]

CAS No. :2683-35-4 MDL No. :MFCD23135477
Formula : C6H5Br2NO Boiling Point : -
Linear Structure Formula :- InChI Key :LYSNTLIRWAIQGH-UHFFFAOYSA-N
M.W : 266.92 Pubchem ID :21766055
Synonyms :

Calculated chemistry of [ 2683-35-4 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.36
TPSA : 22.0 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) : -6.45 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.04
Log Po/w (XLOGP3) : 2.08
Log Po/w (WLOGP) : 1.91
Log Po/w (MLOGP) : 1.31
Log Po/w (SILICOS-IT) : 2.27
Consensus Log Po/w : 1.92

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.25
Solubility : 0.15 mg/ml ; 0.000563 mol/l
Class : Soluble
Log S (Ali) : -2.17
Solubility : 1.8 mg/ml ; 0.00674 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.2
Solubility : 0.168 mg/ml ; 0.000631 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.63

Safety of [ 2683-35-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 2683-35-4 ]

* 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 [ 2683-35-4 ]
  • Downstream synthetic route of [ 2683-35-4 ]

[ 2683-35-4 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 25813-24-5 ]
  • [ 74-88-4 ]
  • [ 2683-35-4 ]
YieldReaction ConditionsOperation in experiment
91% for 12 h; Reflux General procedure: Methyl iodide (4 mmol; 2 equiv.) was added to a solution of 1 (2 mmol) in various solvents (15 ml) and the mixture was refluxed overnight. The reaction was monitored by TLC. After completion, the solvent was removed under reduced pressure and the residue was purified by column chromatography (EtOAc: MeOH, 20:1→5:1) to obtain the products.
Reference: [1] Synthetic Communications, 2017, vol. 47, # 9, p. 872 - 877
  • 2
  • [ 25813-24-5 ]
  • [ 75-03-6 ]
  • [ 2683-35-4 ]
  • [ 90110-13-7 ]
Reference: [1] Synthetic Communications, 2017, vol. 47, # 9, p. 872 - 877
  • 3
  • [ 75-30-9 ]
  • [ 25813-24-5 ]
  • [ 2683-35-4 ]
Reference: [1] Synthetic Communications, 2017, vol. 47, # 9, p. 872 - 877
  • 4
  • [ 25813-25-6 ]
  • [ 74-88-4 ]
  • [ 2683-35-4 ]
Reference: [1] Yakugaku Zasshi, 1952, vol. 72, p. 274[2] Chem.Abstr., 1953, p. 6416
  • 5
  • [ 872-50-4 ]
  • [ 2683-35-4 ]
Reference: [1] Monatshefte fuer Chemie, 1885, vol. 6, p. 312
  • 6
  • [ 87875-76-1 ]
  • [ 2683-35-4 ]
Reference: [1] Canadian Journal of Chemistry, 1983, vol. 61, p. 2556 - 2562
  • 7
  • [ 87875-78-3 ]
  • [ 2683-35-4 ]
  • [ 87875-77-2 ]
Reference: [1] Canadian Journal of Chemistry, 1983, vol. 61, p. 2556 - 2562
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