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[ CAS No. 23667-06-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 23667-06-3
Chemical Structure| 23667-06-3
Structure of 23667-06-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 23667-06-3 ]

CAS No. :23667-06-3 MDL No. :MFCD07780654
Formula : C9H12BrN Boiling Point : -
Linear Structure Formula :- InChI Key :WHDJFGXRKRLPJK-UHFFFAOYSA-N
M.W : 214.10 Pubchem ID :13156670
Synonyms :

Calculated chemistry of [ 23667-06-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 1
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 53.31
TPSA : 3.24 ?2

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) : -5.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.54
Log Po/w (XLOGP3) : 3.1
Log Po/w (WLOGP) : 2.82
Log Po/w (MLOGP) : 3.17
Log Po/w (SILICOS-IT) : 2.53
Consensus Log Po/w : 2.83

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.46
Solubility : 0.0746 mg/ml ; 0.000348 mol/l
Class : Soluble
Log S (Ali) : -2.84
Solubility : 0.312 mg/ml ; 0.00146 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.75
Solubility : 0.0377 mg/ml ; 0.000176 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.35

Safety of [ 23667-06-3 ]

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

Application In Synthesis of [ 23667-06-3 ]

* 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 [ 23667-06-3 ]

[ 23667-06-3 ] Synthesis Path-Upstream   1~9

  • 1
  • [ 99-97-8 ]
  • [ 23667-06-3 ]
YieldReaction ConditionsOperation in experiment
88% at 70℃; for 4 h; General procedure: In a round-bottomed flask, the substrate (1 mmol) and aqueous HBr(48percent) (1 mL) were mixed in DMSO (1 mL). The mixture was stirredat corresponding temperature for 1–4 h. After cooling to roomtemperature, the reaction was adjusted to pH 7–8 with aqueous NaOHsolution (4 M). Then the mixture was washed twice with EtOAc, andthe combined organic extracts were dried, filtered and concentratedunder reduced pressure to give bromination products.
Reference: [1] Journal of Chemical Research, 2014, vol. 38, # 10, p. 593 - 596
[2] Synthesis, 2009, # 21, p. 3672 - 3676
[3] Synthetic Communications, 2010, vol. 40, # 19, p. 2954 - 2962
[4] Tetrahedron Letters, 2007, vol. 48, # 45, p. 7969 - 7973
[5] Chemische Berichte, 1908, vol. 41, p. 2117[6] Chemische Berichte, 1909, vol. 42, p. 2056
[7] Justus Liebigs Annalen der Chemie, 1906, vol. 346, p. 195[8] Chemische Berichte, 1904, vol. 37, p. 2342
[9] Chemische Berichte, 1908, vol. 41, p. 2117[10] Chemische Berichte, 1909, vol. 42, p. 2056
[11] Justus Liebigs Annalen der Chemie, 1906, vol. 346, p. 195[12] Chemische Berichte, 1904, vol. 37, p. 2342
[13] Patent: US1777266, 1926, ,
[14] Chemische Berichte, 1960, vol. 93, p. 1310 - 1318
  • 2
  • [ 583-68-6 ]
  • [ 74-88-4 ]
  • [ 23667-06-3 ]
Reference: [1] Angewandte Chemie - International Edition, 2017, vol. 56, # 45, p. 14272 - 14276
  • 3
  • [ 50-00-0 ]
  • [ 6968-24-7 ]
  • [ 23667-06-3 ]
Reference: [1] Journal of the American Chemical Society, 1940, vol. 62, p. 2159
  • 4
  • [ 614-83-5 ]
  • [ 23667-06-3 ]
Reference: [1] Chemische Berichte, 1983, vol. 116, # 10, p. 3375 - 3405
  • 5
  • [ 87995-51-5 ]
  • [ 23667-06-3 ]
Reference: [1] Chemische Berichte, 1983, vol. 116, # 10, p. 3375 - 3405
  • 6
  • [ 81090-31-5 ]
  • [ 74-88-4 ]
  • [ 23667-06-3 ]
Reference: [1] Chemische Berichte, 1983, vol. 116, # 10, p. 3375 - 3405
  • 7
  • [ 64-19-7 ]
  • [ 99-97-8 ]
  • [ 23667-06-3 ]
Reference: [1] Chemische Berichte, 1908, vol. 41, p. 2117[2] Chemische Berichte, 1909, vol. 42, p. 2056
[3] Justus Liebigs Annalen der Chemie, 1906, vol. 346, p. 195[4] Chemische Berichte, 1904, vol. 37, p. 2342
  • 8
  • [ 67-66-3 ]
  • [ 99-97-8 ]
  • [ 23667-06-3 ]
Reference: [1] Chemische Berichte, 1908, vol. 41, p. 2117[2] Chemische Berichte, 1909, vol. 42, p. 2056
[3] Justus Liebigs Annalen der Chemie, 1906, vol. 346, p. 195[4] Chemische Berichte, 1904, vol. 37, p. 2342
  • 9
  • [ 7664-93-9 ]
  • [ 23667-06-3 ]
Reference: [1] Chemische Berichte, 1908, vol. 41, p. 2117[2] Chemische Berichte, 1909, vol. 42, p. 2056
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