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[ CAS No. 69975-65-1 ] {[proInfo.proName]}

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Chemical Structure| 69975-65-1
Chemical Structure| 69975-65-1
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Quality Control of [ 69975-65-1 ]

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Product Citations

Product Details of [ 69975-65-1 ]

CAS No. :69975-65-1 MDL No. :MFCD00100747
Formula : C9H9NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :UOJCPAAEKXNPQT-UHFFFAOYSA-N
M.W : 147.17 Pubchem ID :312895
Synonyms :

Calculated chemistry of [ 69975-65-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.89
TPSA : 43.09 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.31
Log Po/w (XLOGP3) : 0.98
Log Po/w (WLOGP) : 1.41
Log Po/w (MLOGP) : 1.05
Log Po/w (SILICOS-IT) : 2.04
Consensus Log Po/w : 1.36

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.77
Solubility : 2.48 mg/ml ; 0.0168 mol/l
Class : Very soluble
Log S (Ali) : -1.47
Solubility : 4.95 mg/ml ; 0.0336 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.74
Solubility : 0.27 mg/ml ; 0.00184 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.38

Safety of [ 69975-65-1 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 69975-65-1 ]

* 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 [ 69975-65-1 ]
  • Downstream synthetic route of [ 69975-65-1 ]

[ 69975-65-1 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 24623-25-4 ]
  • [ 24623-24-3 ]
  • [ 51135-91-2 ]
  • [ 69975-65-1 ]
YieldReaction ConditionsOperation in experiment
87% With ammonium chloride In ethanol at 90℃; for 1 h; EXAMPLE 129B 6-amino-1-indanone [0367] A solution of Example 129A (19.68 g, 111 mmol) in ethanol (111 mL) was treated sequentially with iron powder (43.0 g, 770 mmol) and solid ammonium chloride (3.70 g, 69.2 mmol). The resulting suspension was stirred at 90° C. for 1 hour, cooled to room temperature, diluted with brine, and extracted with diethyl ether (4.x.100 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated to provide the desired product as a 6:1 mixture of 6-amino- and 4-amino-1-indanone (14.20 g, 87percent). 1H NMR (300 MHz, DMSO-d6, 6-amino-1-indanone) δ 7.21 (d, 1H), 6.92 (dd, 1H), 6.75 (d, 1H), 5.27 (br s, 2H), 2.90 (t, 2H), 2.54 (m, 2H); 1H NMR (300 MHz, DMSO-d6), 4-amino-1-indanone) δ 7.10 (t, 1H), 6.81 (m, 2H), 2.80 (m, 2H), 2.59 (m, 2H).
Reference: [1] Patent: US2004/167128, 2004, A1, . Location in patent: Page 39
  • 2
  • [ 83-33-0 ]
  • [ 51135-91-2 ]
  • [ 69975-65-1 ]
Reference: [1] Journal of the Chemical Society, 1923, vol. 123, p. 1482,1508
  • 3
  • [ 69975-65-1 ]
  • [ 681246-49-1 ]
YieldReaction ConditionsOperation in experiment
63% With bromine In DMF (N,N-dimethyl-formamide); chloroform for 1 h; EXAMPLE 129C 6-amino-7-bromo-1-indanone [0368] A solution of Example 129B (2.0516 g, 13.94 mmol) in 9:1 CHCl3.DMF (52 mL) was slowly treated with Br2 (0.71 mL, 13.94 mmol), stirred for 1 hour, and filtered. The filter cake was dried under vacuum to provide the desired product (2.7127 g, 63percent). MS (ESI(+)) m/e 226, 228 (M+H)+; MS (ESI(-)) m/e 225, 227 (M-H)-; 1H NMR (300 MHz, DMSO-d6) δ 7.28 (dt, 1H), 7.17 (d, 1H), 5.87 (br s, 3H), 2.89 (m, 2H), 2.62 (m, 2H).
Reference: [1] Patent: US2004/167128, 2004, A1, . Location in patent: Page 40
[2] Patent: WO2009/10260, 2009, A2, . Location in patent: Page/Page column 58
[3] Patent: US2010/273830, 2010, A1, . Location in patent: Page/Page column 33
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