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[ CAS No. 273-09-6 ] {[proInfo.proName]}

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Chemical Structure| 273-09-6
Chemical Structure| 273-09-6
Structure of 273-09-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 273-09-6 ]

CAS No. :273-09-6 MDL No. :MFCD00068064
Formula : C6H4N2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :AWBOSXFRPFZLOP-UHFFFAOYSA-N
M.W : 120.11 Pubchem ID :67501
Synonyms :

Calculated chemistry of [ 273-09-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 31.8
TPSA : 38.92 ?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) : -5.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.79
Log Po/w (XLOGP3) : 1.69
Log Po/w (WLOGP) : 1.22
Log Po/w (MLOGP) : 0.16
Log Po/w (SILICOS-IT) : 1.54
Consensus Log Po/w : 1.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.39
Solubility : 0.49 mg/ml ; 0.00408 mol/l
Class : Soluble
Log S (Ali) : -2.12
Solubility : 0.906 mg/ml ; 0.00755 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.49
Solubility : 0.387 mg/ml ; 0.00322 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.29

Safety of [ 273-09-6 ]

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

Application In Synthesis of [ 273-09-6 ]

* 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 [ 273-09-6 ]

[ 273-09-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 273-09-6 ]
  • [ 54286-63-4 ]
YieldReaction ConditionsOperation in experiment
25% at 90℃; for 2 h; Reflux Benzo[c][l,2,5]oxadiazole (2.5 g, 21 mmol) was heated to 90 0C with iron powder (0.23 g, 4.2 mmol). The molten liquid was then treated with bromine (3.2 ml, 62 mmol) and refluxed for 2 h. The resultant solution was poured onto ice and the precipitate filtered. The precipitate was then mixed with aq. NaHCO3, stirred for 15 min and filtered. Flash chromatography (n-hexane/EtOAc 9:1) afforded the title compound as an orange solid (1.5 g, 25 percent); m.p. 88 - 92 0C; vmax(thin film) 1514, 1344, 1201, 1026, 954, 871, 841 cm-1; δH(500 MHz, CDCl3) 7.51 (2H, s, Ar-H); δC (126 MHz, CDCl3) 149.6 (C=N), 134.4 (Ar-Q, 108.9 (ipso-Ai-Q; m/z (EI) 280([81'81Br]M+, 6percent), 278 ([81^9Br]M+, 8percent), 276 ([79^9Br]M+, 6percent), 250 (5percent), 248 (10percent), 246 (7percent), 197 (5percent); all data agree with those reported in the literature.
Reference: [1] Journal of Materials Chemistry C, 2015, vol. 3, # 5, p. 973 - 976
[2] New Journal of Chemistry, 2012, vol. 36, # 3, p. 550 - 553
[3] Journal of the American Chemical Society, 2008, vol. 130, # 2, p. 732 - 742
[4] Journal of Materials Chemistry C, 2015, vol. 3, # 35, p. 9145 - 9153
[5] Patent: WO2009/34396, 2009, A2, . Location in patent: Page/Page column 91-92
[6] Journal of the Chemical Society, 1931, p. 3308
[7] Dyes and Pigments, 2012, vol. 95, # 2, p. 229 - 235
[8] Journal of Polymer Science, Part A: Polymer Chemistry, 2012, vol. 50, # 19, p. 3996 - 4003
[9] Synthetic Communications, 2016, vol. 46, # 12, p. 1052 - 1061
[10] RSC Advances, 2017, vol. 7, # 33, p. 20440 - 20450
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