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[ CAS No. 16004-15-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 16004-15-2
Chemical Structure| 16004-15-2
Structure of 16004-15-2 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Zehuan Huang ; Xiaoyi Chen ; Stephen J. K. O’Neill , et al. DOI: PubMed ID:

Abstract: Supramolecular polymer networks are non-covalently crosslinked soft materials that exhibit unique mechanical features such as self-healing, high toughness and stretchability. Previous studies have focused on optimizing such properties using fast-dissociative crosslinks (that is, for an aqueous system, dissociation rate constant kd?>?10?s?1). Herein, we describe non-covalent crosslinkers with slow, tuneable dissociation kinetics (kd?

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Product Details of [ 16004-15-2 ]

CAS No. :16004-15-2 MDL No. :MFCD00209656
Formula : C7H6BrI Boiling Point : No data available
Linear Structure Formula :- InChI Key :BQTRMYJYYNQQGK-UHFFFAOYSA-N
M.W : 296.93 Pubchem ID :954258
Synonyms :

Calculated chemistry of [ 16004-15-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 52.0
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.4
Log Po/w (XLOGP3) : 4.02
Log Po/w (WLOGP) : 3.03
Log Po/w (MLOGP) : 3.98
Log Po/w (SILICOS-IT) : 3.82
Consensus Log Po/w : 3.45

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.64
Solubility : 0.00679 mg/ml ; 0.0000229 mol/l
Class : Moderately soluble
Log S (Ali) : -3.72
Solubility : 0.0562 mg/ml ; 0.000189 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.59
Solubility : 0.00756 mg/ml ; 0.0000255 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.22

Safety of [ 16004-15-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 16004-15-2 ]

* 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.

  • Downstream synthetic route of [ 16004-15-2 ]

[ 16004-15-2 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 16004-15-2 ]
  • [ 39987-25-2 ]
  • [ 6096-66-8 ]
  • 2
  • [ 6374-91-0 ]
  • [ 16004-15-2 ]
  • 5,7-dibromo-N-(p-iodobenzyl)isatin [ No CAS ]
  • 3
  • [ 2882-15-7 ]
  • [ 16004-15-2 ]
  • [ 1217549-14-8 ]
  • 4
  • [ 16004-15-2 ]
  • [ 2243-58-5 ]
  • 1-(4-iodobenzyl)-1-(naphthalen-2-yl)hydrazine [ No CAS ]
  • 5
  • [ 16004-15-2 ]
  • [ 66521-66-2 ]
  • N-(4-iodobenzyl)-4-(pyridin-3-yl)pyrimidin-2-amine [ No CAS ]
  • 6
  • [ 198211-38-0 ]
  • [ 16004-15-2 ]
  • (2R)-4-(6-((4-((6-amino-3-azabicyclo[3.1.0]hexan-3-yl)methyl)phenyl)ethynyl)-3-oxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl)-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide [ No CAS ]
  • 7
  • [ 198211-38-0 ]
  • [ 16004-15-2 ]
  • tert-butyl (3-(4-iodobenzyl)-3-azabicyclo[3.1.0]hexan-6-yl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
61% With potassium carbonate; potassium iodide; In acetonitrile; at 80℃; for 1h; Preparation G: tert-butyl (3-(4-iodobenzyl)-3-azabicyclo[3.1.0]hexan- 6-yl)carbamate: To a stirred solution of <strong>[198211-38-0]6-(Boc-amino)-3-azabicyclo[3.1.0]hexane</strong> (0.250 g, 1.26 mmol) in MeCN (10 mL) were added K2C03 (0.52 g, 3.78 mmol), 4-iodobenzyl bromide (0.449 g, 1.51 mmol) and KI (0.006 g, 0.0378 mmol). The resulting reaction mixture was heated at 80 C for 1 h. The solvent was removed under reduced pressure and the residue was partitioned between DCM (100 mL) and water (25 mL). The org. layer was separated and the aq. layer was extracted with DCM (2 x 25 mL). The combined org. layers were washed with water (2 x 25 mL). The evaporation residue was purified by CC (DCM-MeOH) to afford the title compound as a beige solid (0.32 g, 61% yield). XH NMR (i/6-DMSO) delta: 7.66 (d, J = 8.3 Hz, 2H); 7.06 (d, J = 8.3 Hz, 2H); 6.90 (m, 1H); 3.48 (s, 2H); 2.88 (d, J = 8.8 Hz, 2H); 2.68 (d, J = 0.3 Hz, 1H); 2.30 (d, J = 8.4 Hz, 2H); 1.37 (s, 9H). MS (ESI, m/z): 414.96 [M+H+] for CnHnNzOzI; tR = 0.68 min.
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