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[ CAS No. 40000-20-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 40000-20-2
Chemical Structure| 40000-20-2
Structure of 40000-20-2 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 40000-20-2 ]

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Product Details of [ 40000-20-2 ]

CAS No. :40000-20-2 MDL No. :MFCD00046903
Formula : C12H7BrN2 Boiling Point : -
Linear Structure Formula :- InChI Key :GWKGPQCKIBRXGW-UHFFFAOYSA-N
M.W : 259.10 Pubchem ID :148335
Synonyms :

Calculated chemistry of [ 40000-20-2 ]

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 14
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 64.74
TPSA : 25.78 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.02
Log Po/w (XLOGP3) : 3.15
Log Po/w (WLOGP) : 3.55
Log Po/w (MLOGP) : 2.54
Log Po/w (SILICOS-IT) : 3.62
Consensus Log Po/w : 2.97

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.12
Solubility : 0.0196 mg/ml ; 0.0000756 mol/l
Class : Moderately soluble
Log S (Ali) : -3.36
Solubility : 0.113 mg/ml ; 0.000435 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.86
Solubility : 0.000358 mg/ml ; 0.00000138 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.78

Safety of [ 40000-20-2 ]

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 [ 40000-20-2 ]

* 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.

  • Upstream synthesis route of [ 40000-20-2 ]
  • Downstream synthetic route of [ 40000-20-2 ]

[ 40000-20-2 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 66-71-7 ]
  • [ 40000-20-2 ]
Reference: [1] Crystal Growth and Design, 2016, vol. 16, # 12, p. 6992 - 6999
[2] Inorganic Chemistry, 2010, vol. 49, # 6, p. 2889 - 2900
[3] Dalton Transactions, 2007, # 31, p. 3421 - 3426
[4] European Journal of Inorganic Chemistry, 2017, vol. 2017, # 32, p. 3799 - 3810
[5] Chemical Communications, 2015, vol. 51, # 97, p. 17269 - 17272
[6] Inorganic Chemistry, 2018,
[7] Antimicrobial Agents and Chemotherapy, 2017, vol. 61, # 11,
[8] Molecules, 2011, vol. 16, # 10, p. 8353 - 8367
[9] Synthesis (Germany), 2013, vol. 45, # 6, p. 753 - 758
[10] Journal of the American Chemical Society, 2014, vol. 136, # 22, p. 7861 - 7864
[11] Journal of the American Chemical Society, 2014, vol. 136, # 43, p. 15300 - 15309
[12] European Journal of Inorganic Chemistry, 2017, vol. 2017, # 3, p. 623 - 629
  • 2
  • [ 53472-18-7 ]
  • [ 504-63-2 ]
  • [ 40000-20-2 ]
Reference: [1] Patent: CN108530443, 2018, A, . Location in patent: Paragraph 0058; 0060-0062
  • 3
  • [ 57339-57-8 ]
  • [ 56-81-5 ]
  • [ 40000-20-2 ]
Reference: [1] Journal of the American Chemical Society, 1944, vol. 66, p. 396
  • 4
  • [ 41119-20-4 ]
  • [ 40000-20-2 ]
Reference: [1] Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1989, vol. 85, # 11, p. 3733 - 3746
  • 5
  • [ 53472-18-7 ]
  • [ 56-81-5 ]
  • [ 40000-20-2 ]
Reference: [1] Journal of the Chemical Society, 1946, p. 155
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