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[ CAS No. 70173-54-5 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 70173-54-5
Chemical Structure| 70173-54-5
Chemical Structure| 70173-54-5
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Product Details of [ 70173-54-5 ]

CAS No. :70173-54-5 MDL No. :MFCD03001720
Formula : C12H14BrN Boiling Point : -
Linear Structure Formula :- InChI Key :PVTRKHJBWSTNOI-UHFFFAOYSA-N
M.W : 252.15 Pubchem ID :2757027
Synonyms :

Calculated chemistry of [ 70173-54-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 66.6
TPSA : 3.24 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.34 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.77
Log Po/w (XLOGP3) : 3.52
Log Po/w (WLOGP) : 2.77
Log Po/w (MLOGP) : 3.61
Log Po/w (SILICOS-IT) : 3.66
Consensus Log Po/w : 3.27

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.94
Solubility : 0.0291 mg/ml ; 0.000115 mol/l
Class : Soluble
Log S (Ali) : -3.27
Solubility : 0.135 mg/ml ; 0.000535 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.25
Solubility : 0.0142 mg/ml ; 0.0000562 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.97

Safety of [ 70173-54-5 ]

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 [ 70173-54-5 ]

* 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 [ 70173-54-5 ]
  • Downstream synthetic route of [ 70173-54-5 ]

[ 70173-54-5 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 479-59-4 ]
  • [ 70173-54-5 ]
YieldReaction ConditionsOperation in experiment
80% With N-Bromosuccinimide In N,N-dimethyl-formamide at 20℃; for 5 h; A 10mL DMF solution of julolidine (675 mg, 3.90 mmol) and NBS(832 mg, 4.68 mmol) was stirred for 5 h at room temperature. Thecrude product was purified by silica column chromatography(hexane/methylene chloride3/1) to obtain JeBr (786 mg, 80percent) as ared oil. 1H NMR (500 MHz, CDCl3): d/ppm: 6.87 (s, 2H), 3.10 (t, 4H,J5.50 Hz), 2.70 (t, 4H, J6.35 Hz),1.94 (m, 4H). 13CNMR(500 MHz,CDCl3): d/ppm: 142.0, 129.3, 123.7, 107.3, 50.0, 27.6, 21.9. IR (KBr,cm1): 3045, 2935, 2836,1581,1506,1462,1446,1310. TOFMS-EI (m/z): calcd. for (M) C12H14NBr: 251.0310, found: 251.0309.
Reference: [1] Chemical and Pharmaceutical Bulletin, 1984, vol. 32, # 5, p. 1770 - 1779
[2] Canadian Journal of Chemistry, 2009, vol. 87, # 2, p. 440 - 447
[3] Journal of Organic Chemistry, 2011, vol. 76, # 22, p. 9391 - 9408
[4] Dyes and Pigments, 2013, vol. 99, # 3, p. 653 - 660
[5] European Journal of Organic Chemistry, 2011, # 30, p. 6100 - 6109
[6] Tetrahedron, 2007, vol. 63, # 1, p. 103 - 114
[7] Journal of Organic Chemistry, 1952, vol. 17, p. 1281,1288
[8] Chemical Communications, 2010, vol. 46, # 36, p. 6666 - 6668
[9] Patent: KR2016/99254, 2016, A, . Location in patent: Paragraph 0081; 0082; 0084; 0085
  • 2
  • [ 635-46-1 ]
  • [ 70173-54-5 ]
Reference: [1] European Journal of Organic Chemistry, 2011, # 30, p. 6100 - 6109
  • 3
  • [ 76859-18-2 ]
  • [ 70173-54-5 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1984, vol. 32, # 5, p. 1770 - 1779
  • 4
  • [ 93033-85-3 ]
  • [ 70173-54-5 ]
  • [ 76859-15-9 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1984, vol. 32, # 5, p. 1770 - 1779
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