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[ CAS No. 42872-74-2 ] {[proInfo.proName]}

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Chemical Structure| 42872-74-2
Chemical Structure| 42872-74-2
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Product Details of [ 42872-74-2 ]

CAS No. :42872-74-2 MDL No. :MFCD06797818
Formula : C8H6BrN Boiling Point : -
Linear Structure Formula :- InChI Key :VXUMRYMTYKDWMO-UHFFFAOYSA-N
M.W : 196.04 Pubchem ID :14004840
Synonyms :

Calculated chemistry of [ 42872-74-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.82
TPSA : 23.79 ?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) : -5.58 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 2.7
Log Po/w (WLOGP) : 2.63
Log Po/w (MLOGP) : 2.52
Log Po/w (SILICOS-IT) : 2.94
Consensus Log Po/w : 2.58

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.2
Solubility : 0.124 mg/ml ; 0.00063 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.275 mg/ml ; 0.0014 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.73
Solubility : 0.0368 mg/ml ; 0.000188 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.89

Safety of [ 42872-74-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280 UN#:N/A
Hazard Statements:H302+H312+H332 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 42872-74-2 ]

* 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 [ 42872-74-2 ]
  • Downstream synthetic route of [ 42872-74-2 ]

[ 42872-74-2 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 42872-74-2 ]
  • [ 89892-39-7 ]
YieldReaction ConditionsOperation in experiment
95% With N-Bromosuccinimide; dibenzoyl peroxide In tetrachloromethane at 85℃; for 18 h; Inert atmosphere To a stirred solution of 3-bromo-4-methyl-benzonitrile (2 g, 10.2014 mmol, 100 mass percent) in carbon tetrachloride (20 ml_, 100 mass percent) under argon, was added NBS (2.2 g., 12.2417 mmol, 99 mass percent) and benzoyl peroxide (0.123 g., 0.5101 mmol, 100 mass percent). The mixture was heated to 85°C for 18h. The reaction mass was diluted with water (50 ml) and extracted with ethyl acetate. Organics were washed again with water and brine, dried and evaporated to afford 3-bromo-4-(bromomethyl) benzonitrile (1.2 g, 4.4 mmol, 90 mass percent, 95percent Yield) as an off white solid solid. H NMR (400 MHz, chloroform-c) δ ppm 3.89 - 4.01 (m, 2 H) 6.61 - 6.77 (m, 1 H) 6.92 - 7.07 (m, 2 H) LCMS: RT 1.12-1.49 Min 274 [M+H] +
52.5% With N-Bromosuccinimide; dibenzoyl peroxide In tetrachloromethaneInert atmosphere; Reflux The compound 57 (804 mg, 4.04 mmol) was dissolved in carbon tetrachloride (8 mL), and then added with NBS (730 mg, 4.10 mmol) and benzoyl peroxide (7 mg, 0.0289 mmol). The resulting mixture was heated under the protection of nitrogen until reflux occurred, and was stirred overnight. The mixture was cooled to room temperature, filtered to remove insoluble substances and distilled under reduced pressure to remove the solvent, then dissolved in ethyl acetate (30 mL) and respectively washed with water (10 mL) and saturated saline solution (10 mL). After the solvent was removed by means of reduced pressure distillation, the resulting product was purified by using a silica column (200 to 300 mesh silica gel, ethyl acetate/petroleum ether=1/35 for elution) to obtain 3-bromo-4-cyanobenzyl bromide (58) (583 mg), with a yield of 52.5percent.
Reference: [1] Patent: WO2016/113303, 2016, A1, . Location in patent: Page/Page column 41
[2] Journal of the American Chemical Society, 2017, vol. 139, # 2, p. 829 - 835
[3] Journal of the American Chemical Society, 2009, vol. 131, # 39, p. 13908 - 13909
[4] Patent: EP2927219, 2015, A1, . Location in patent: Paragraph 0130; 0132
[5] Journal of Organic Chemistry, 1964, vol. 29, p. 2034 - 2036
[6] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 21, p. 3821 - 3825
[7] Patent: WO2010/85581, 2010, A1, . Location in patent: Page/Page column 71-72
[8] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 2, p. 644 - 651
[9] Patent: WO2011/22337, 2011, A1, . Location in patent: Page/Page column 104
  • 2
  • [ 42872-74-2 ]
  • [ 956218-04-5 ]
Reference: [1] Synlett, 2007, # 14, p. 2179 - 2184
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